A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4691n100



Internal ID22790778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21745401..21767774hg38UCSC Ensembl
chr3:21786893..21809266hg19UCSC Ensembl
chr3:21761897..21784270hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3822374
hg1922374
hg1822374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015075, nsv1011725
Samples
Known GenesZNF385D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4691n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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