A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4690n100



Internal ID22790777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21199919..21315784hg38UCSC Ensembl
chr3:21241411..21357276hg19UCSC Ensembl
chr3:21216415..21332280hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38115866
hg19115866
hg18115866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998571, nsv1002386, nsv1003084, nsv1010472, nsv997987, nsv1007017, nsv1013139, nsv1004773, nsv1008438, nsv1010060, nsv1012826, nsv1003641, nsv1014491, nsv1014872, nsv1004536, nsv1012654, nsv1004366, nsv1007987
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)dgv4690n100
Frequency
Sample Size11257
Observed Gain40
Observed Loss0
Observed Complex0
Frequencyn/a


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