A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4564n54



Internal ID22772459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61950998..62021218hg38UCSC Ensembl
chr15:62243197..62313417hg19UCSC Ensembl
chr15:60030489..60100709hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3870221
hg1970221
hg1870221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569651, nsv569650, nsv569649
Samples
Known GenesVPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4564n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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