A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655233



Internal ID15045199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29114494..29120892hg38UCSC Ensembl
Innerchr15:29406697..29413095hg19UCSC Ensembl
Innerchr15:27193989..27200387hg18UCSC Ensembl
Innerchr15:27193989..27200387hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg386399
hg196399
hg186399
hg176399
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)nssv655233
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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