A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526666



Internal ID15107273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102824573..102837723hg38UCSC Ensembl
Innerchr10:104584330..104597480hg19UCSC Ensembl
Innerchr10:104574320..104587470hg18UCSC Ensembl
Innerchr10:104574320..104587470hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3813151
hg1913151
hg1813151
hg1713151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702995
Samples
Known GenesCYP17A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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