Variant #0000129140 (NC_000011.9:g.(pter_196966)_(7001800_10700000)dup)

Individual ID 00080104
Chromosome 11
Allele Maternal (confirmed)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.(pter_196966)_(7001800_10700000)dup
DNA change (hg38) -
Published as arr[hg18] 11p15.5-p15.4(186,966-6,958,376)x3 mat
ISCN arr[hg19] 11p15.5-p15.4(196,966-7,001,800)x3 mat
DB-ID chr11_000459
Variant remarks duplication
Reference PubMed: Cardarelli 2010, PubMed: Fokstuen 2013, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Zeynep Tümer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2016-09-01 17:30:25 +02:00 (CEST)
Date last edited 2020-10-01 16:53:33 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000080195 DNA arrayCNV; FISH; STR - - - 1 Zeynep Tümer


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