A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4658n100



Internal ID22790745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5327116..5648141hg38UCSC Ensembl
chr3:5368801..5689828hg19UCSC Ensembl
chr3:5343801..5664828hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38321026
hg19321028
hg18321028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006549, nsv1009089, nsv1015094
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)dgv4658n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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