A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4648n100



Internal ID20156264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4066953..4172280hg38UCSC Ensembl
chr3:4108637..4213964hg19UCSC Ensembl
chr3:4083637..4188964hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38105328
hg19105328
hg18105328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006983, nsv1012637, nsv1005720
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)dgv4648n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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