A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4436n54



Internal ID22772331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31483278..31484086hg38UCSC Ensembl
chr15:31775481..31776289hg19UCSC Ensembl
chr15:29562773..29563581hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568814, nsv568804, nsv568809, nsv568815, nsv568808, nsv568807
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4436n54
Frequency
Sample Size17421
Observed Gain20
Observed Loss18
Observed Complex0
Frequencyn/a


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