A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699009



Internal ID15435661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89146733..89162497hg38UCSC Ensembl
Innerchr15:89689964..89705728hg19UCSC Ensembl
Innerchr15:87490968..87506732hg18UCSC Ensembl
Innerchr15:87490968..87506732hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3815765
hg1915765
hg1815765
hg1715765
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523275
Supporting Variants
Samples
Known GenesABHD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699009
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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