A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4437n54



Internal ID22772332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31483278..31484300hg38UCSC Ensembl
chr15:31775481..31776503hg19UCSC Ensembl
chr15:29562773..29563795hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381023
hg191023
hg181023
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568817, nsv568821, nsv568820, nsv568806
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4437n54
Frequency
Sample Size17421
Observed Gain16
Observed Loss9
Observed Complex0
Frequencyn/a


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