A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4692n100



Internal ID22790779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21754716..21767774hg38UCSC Ensembl
chr3:21796208..21809266hg19UCSC Ensembl
chr3:21771212..21784270hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3813059
hg1913059
hg1813059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003040, nsv1006809
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)dgv4692n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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