A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4302n100



Internal ID20155918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33413503..33558912hg38UCSC Ensembl
chr20:32001309..32146718hg19UCSC Ensembl
chr20:31464970..31610379hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38145410
hg19145410
hg18145410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063864, nsv1058357
Samples
Known GenesCBFA2T2, SNTA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4302n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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