A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568665



Internal ID16009388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28065828..28123823hg38UCSC Ensembl
Innerchr15:28310974..28368969hg19UCSC Ensembl
Innerchr15:25984569..26042564hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3857996
hg1957996
hg1857996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839291
Samples
Known GenesHERC2, OCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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