A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4682n100



Internal ID22790769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11881906..11912460hg38UCSC Ensembl
chr3:11923380..11953934hg19UCSC Ensembl
chr3:11898380..11928934hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3830555
hg1930555
hg1830555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009661, nsv1000702, nsv1004959, nsv1010823, nsv998469, nsv1014141, nsv1013305
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)dgv4682n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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