A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516171



Internal ID15443464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63858789..64362111hg38UCSC Ensembl
Innerchr13:64432922..64936243hg19UCSC Ensembl
Innerchr13:63330923..63834244hg18UCSC Ensembl
Innerchr13:63330923..63834244hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38503323
hg19503322
hg18503322
hg17503322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666612, nssv675829, nssv677959, nssv658764, nssv658043, nssv658837, nssv699212
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516171
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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