A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568675



Internal ID16009398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29035149..29916451hg38UCSC Ensembl
Innerchr15:29327352..30208654hg19UCSC Ensembl
Innerchr15:27114644..27995946hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38881303
hg19881303
hg18881303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839305
Samples
Known GenesAPBA2, FAM189A1, NDNL2, TJP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568675
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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