A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568802



Internal ID16009525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483187..31483974hg38UCSC Ensembl
Innerchr15:31775390..31776177hg19UCSC Ensembl
Innerchr15:29562682..29563469hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38788
hg19788
hg18788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4435n54
Supporting Variantsnssv839578
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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