A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570303



Internal ID16011026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85282336..85600273hg38UCSC Ensembl
Innerchr15:85825567..86143504hg19UCSC Ensembl
Innerchr15:83626571..83944508hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38317938
hg19317938
hg18317938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n54
Supporting Variantsnssv1149255, nssv847706, nssv847705
Samples1782681216_A
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570303
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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