A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516774



Internal ID15097381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48806283..48806771hg38UCSC Ensembl
Innerchr10:50014328..50014816hg19UCSC Ensembl
Innerchr10:49684334..49684822hg18UCSC Ensembl
Innerchr10:49684334..49684822hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38489
hg19489
hg18489
hg17489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653150, nssv653456
Samples
Known GenesWDFY4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516774
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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