A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4619n54



Internal ID22772514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73367751..73368898hg38UCSC Ensembl
chr15:73660092..73661239hg19UCSC Ensembl
chr15:71447145..71448292hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381148
hg191148
hg181148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569960, nsv569956, nsv569961, nsv569951, nsv569962
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4619n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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