A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570301



Internal ID16011024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85282336..85564521hg38UCSC Ensembl
Innerchr15:85825567..86107752hg19UCSC Ensembl
Innerchr15:83626571..83908756hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38282186
hg19282186
hg18282186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n54
Supporting Variantsnssv847704
Samples
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570301
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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