A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4639n100



Internal ID22790726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3917080..3935472hg38UCSC Ensembl
chr3:3958764..3977156hg19UCSC Ensembl
chr3:3933764..3952156hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3818393
hg1918393
hg1818393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005925, nsv1006862, nsv1007781
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)dgv4639n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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