A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682130



Internal ID15072096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29090260..29146274hg38UCSC Ensembl
Innerchr15:29382463..29438477hg19UCSC Ensembl
Innerchr15:27169755..27225769hg18UCSC Ensembl
Innerchr15:27169755..27225769hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3856015
hg1956015
hg1856015
hg1756015
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515798
Supporting Variants
Samples
Known GenesAPBA2, FAM189A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682130
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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