A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524129



Internal ID15451422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70675215..70690703hg38UCSC Ensembl
Innerchr15:70967554..70983042hg19UCSC Ensembl
Innerchr15:68754608..68770096hg18UCSC Ensembl
Innerchr15:68754608..68770096hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3815489
hg1915489
hg1815489
hg1715489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700007
Samples
Known GenesUACA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524129
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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