A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4654n100



Internal ID20156270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4123660..4237761hg38UCSC Ensembl
chr3:4165344..4279445hg19UCSC Ensembl
chr3:4140344..4254445hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38114102
hg19114102
hg18114102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001367, nsv999653, nsv998608, nsv1000312, nsv1008220
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)dgv4654n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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