A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698481



Internal ID15435133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37251359..37254547hg38UCSC Ensembl
Innerchr15:37543560..37546748hg19UCSC Ensembl
Innerchr15:35330852..35334040hg18UCSC Ensembl
Innerchr15:35330852..35334040hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383189
hg193189
hg183189
hg173189
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522831
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698481
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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