A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4602n100



Internal ID22790689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..66756hg38UCSC Ensembl
chr3:60333..108439hg19UCSC Ensembl
chr3:35333..83439hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3848102
hg1948107
hg1848107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014667, nsv1012870, nsv1008719, nsv1010364, nsv1009455, nsv1006613
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)dgv4602n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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