A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4715n100



Internal ID22790802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34692520..34765179hg38UCSC Ensembl
chr3:34734012..34806671hg19UCSC Ensembl
chr3:34709016..34781675hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3872660
hg1972660
hg1872660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997333, nsv1014239
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)dgv4715n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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