A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570297



Internal ID16011020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85237085..85566351hg38UCSC Ensembl
Innerchr15:85780316..86109582hg19UCSC Ensembl
Innerchr15:83581320..83910586hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38329267
hg19329267
hg18329267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n54
Supporting Variantsnssv847700
Samples
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570297
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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