A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4646n100



Internal ID20156262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4046103..4107492hg38UCSC Ensembl
chr3:4087787..4149176hg19UCSC Ensembl
chr3:4062787..4124176hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3861390
hg1961390
hg1861390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011673, nsv1002795
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)dgv4646n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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