A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568663



Internal ID16009386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27783102..28176880hg38UCSC Ensembl
Innerchr15:28028248..28422026hg19UCSC Ensembl
Innerchr15:25701843..26095621hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38393779
hg19393779
hg18393779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839290
Samples
Known GenesHERC2, OCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568663
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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