A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515726



Internal ID15442783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:218080470..218224238hg38UCSC Ensembl
Innerchr1:218253812..218397580hg19UCSC Ensembl
Innerchr1:216320435..216464203hg18UCSC Ensembl
Innerchr1:214642207..214785975hg17UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38143769
hg19143769
hg18143769
hg17143769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664587, nssv658847
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515726
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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