A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839579



Internal ID15786849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483278..31483920hg38UCSC Ensembl
Innerchr15:31775481..31776123hg19UCSC Ensembl
Innerchr15:29562773..29563415hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38643
hg19643
hg18643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568803
Supporting Variants
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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