A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698892



Internal ID15435544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100462533..100462916hg38UCSC Ensembl
Innerchr15:101002738..101003121hg19UCSC Ensembl
Innerchr15:98820261..98820644hg18UCSC Ensembl
Innerchr15:98820261..98820644hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38384
hg19384
hg18384
hg17384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523179
Supporting Variants
Samples
Known GenesCERS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698892
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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