A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4693n100



Internal ID22790780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21880215..21920801hg38UCSC Ensembl
chr3:21921707..21962293hg19UCSC Ensembl
chr3:21896711..21937297hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3840587
hg1940587
hg1840587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998906, nsv1014821
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)dgv4693n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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