A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4735n100



Internal ID22790822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46760315..46790579hg38UCSC Ensembl
chr3:46801805..46832069hg19UCSC Ensembl
chr3:46776809..46807073hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3830265
hg1930265
hg1830265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006788, nsv1001910
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4735n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss59
Observed Complex0
Frequencyn/a


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