A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4671n100



Internal ID22790758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6262764..6299812hg38UCSC Ensembl
chr3:6304451..6341499hg19UCSC Ensembl
chr3:6279451..6316499hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3837049
hg1937049
hg1837049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012973, nsv1012153, nsv1009500
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)dgv4671n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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