A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8237n54



Internal ID22776132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15802839..15804877hg38UCSC Ensembl
chr3:15844346..15846384hg19UCSC Ensembl
chr3:15819350..15821388hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382039
hg192039
hg182039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589788, nsv589789, nsv589786, nsv589787
Samples
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8237n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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