A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688880



Internal ID15078846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29114494..29120748hg38UCSC Ensembl
Innerchr15:29406697..29412951hg19UCSC Ensembl
Innerchr15:27193989..27200243hg18UCSC Ensembl
Innerchr15:27193989..27200243hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg386255
hg196255
hg186255
hg176255
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)nssv688880
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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