A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676848



Internal ID15066814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29089598..29136885hg38UCSC Ensembl
Innerchr15:29381801..29429088hg19UCSC Ensembl
Innerchr15:27169093..27216380hg18UCSC Ensembl
Innerchr15:27169093..27216380hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3847288
hg1947288
hg1847288
hg1747288
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)nssv676848
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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