A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569153



Internal ID16009876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34757586..34935412hg38UCSC Ensembl
Innerchr15:35049787..35227613hg19UCSC Ensembl
Innerchr15:32837079..33014905hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38177827
hg19177827
hg18177827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149153
Samples1780862252_A
Known GenesACTC1, AQR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569153
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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