A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657612



Internal ID15047578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34450532..34508394hg38UCSC Ensembl
Innerchr15:34742733..34800595hg19UCSC Ensembl
Innerchr15:32530025..32587887hg18UCSC Ensembl
Innerchr15:32530025..32587887hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3857863
hg1957863
hg1857863
hg1757863
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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