A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4652n100



Internal ID22790739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4104499..4295321hg38UCSC Ensembl
chr3:4146183..4337005hg19UCSC Ensembl
chr3:4121183..4312005hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38190823
hg19190823
hg18190823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008570, nsv1006352, nsv997809, nsv1002519, nsv1007955, nsv1014294, nsv1002648, nsv1011061
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)dgv4652n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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