A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4332n100



Internal ID22790419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55122969..55165844hg38UCSC Ensembl
chr20:53739508..53782383hg19UCSC Ensembl
chr20:53172915..53215790hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3842876
hg1942876
hg1842876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066209, nsv1060042, nsv1056446
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)dgv4332n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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