A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517068



Internal ID15097675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76962203..77088880hg38UCSC Ensembl
Innerchr15:77254544..77381222hg19UCSC Ensembl
Innerchr15:75041599..75168277hg18UCSC Ensembl
Innerchr15:75041599..75168277hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38126678
hg19126679
hg18126679
hg17126679
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697047, nssv682226, nssv682321, nssv661383, nssv693432, nssv661834, nssv665263, nssv692990, nssv683277, nssv697169, nssv685115, nssv692684, nssv674633, nssv653725
Samples
Known GenesPSTPIP1, TSPAN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517068
Frequency
Sample Size2026
Observed Gain1
Observed Loss13
Observed Complex0
Frequencyn/a


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