A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4798n100



Internal ID20156414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80470812..80539436hg38UCSC Ensembl
chr3:80519962..80588586hg19UCSC Ensembl
chr3:80602652..80671276hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3868625
hg1968625
hg1868625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001789, nsv1005381
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)dgv4798n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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