A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570302



Internal ID16011025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85282336..85566351hg38UCSC Ensembl
Innerchr15:85825567..86109582hg19UCSC Ensembl
Innerchr15:83626571..83910586hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38284016
hg19284016
hg18284016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n54
Supporting Variantsnssv1149254
Samples1798860114_A
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570302
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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