A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5001n100



Internal ID22791088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184469612..184555921hg38UCSC Ensembl
chr3:184187400..184273709hg19UCSC Ensembl
chr3:185670094..185756403hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3886310
hg1986310
hg1886310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008844, nsv1006724
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)dgv5001n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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