A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8376n54



Internal ID22776271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72730895..72734221hg38UCSC Ensembl
chr3:72780046..72783372hg19UCSC Ensembl
chr3:72862736..72866062hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383327
hg193327
hg183327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590617, nsv590623, nsv590618
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8376n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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