A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570313



Internal ID16011036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85367747..85600205hg38UCSC Ensembl
Innerchr15:85910978..86143436hg19UCSC Ensembl
Innerchr15:83711982..83944440hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38232459
hg19232459
hg18232459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4694n54
Supporting Variantsnssv847718
Samples
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570313
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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