A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697875



Internal ID15434527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94570982..94572860hg38UCSC Ensembl
Innerchr15:95114211..95116089hg19UCSC Ensembl
Innerchr15:92915215..92917093hg18UCSC Ensembl
Innerchr15:92915215..92917093hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381879
hg191879
hg181879
hg171879
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521263
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697875
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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