A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4435n54



Internal ID20137859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31483187..31484140hg38UCSC Ensembl
chr15:31775390..31776343hg19UCSC Ensembl
chr15:29562682..29563635hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38954
hg19954
hg18954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568802, nsv568803, nsv568810
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4435n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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