A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4347n100



Internal ID20155963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64131041..64324788hg38UCSC Ensembl
chr20:62762394..62956141hg19UCSC Ensembl
chr20:62232838..62426585hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38193748
hg19193748
hg18193748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055670, nsv1063896, nsv1067195
Samples
Known GenesLINC00266-1, MYT1, PCMTD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4347n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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