A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570299



Internal ID16011022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85272357..85600205hg38UCSC Ensembl
Innerchr15:85815588..86143436hg19UCSC Ensembl
Innerchr15:83616592..83944440hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38327849
hg19327849
hg18327849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n54
Supporting Variantsnssv847702
Samples
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570299
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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