A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526692



Internal ID15453985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68202362..68228417hg38UCSC Ensembl
Innerchr6:68912254..68938309hg19UCSC Ensembl
Innerchr6:68968975..68995030hg18UCSC Ensembl
Innerchr6:68968975..68995030hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3826056
hg1926056
hg1826056
hg1726056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703029
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526692
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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