A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4800n100



Internal ID22790887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82659093..82719539hg38UCSC Ensembl
chr3:82708244..82768690hg19UCSC Ensembl
chr3:82790934..82851380hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3860447
hg1960447
hg1860447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010803, nsv1008386
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)dgv4800n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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