A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4338n100



Internal ID22790425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60883504..61013529hg38UCSC Ensembl
chr20:59458560..59588585hg19UCSC Ensembl
chr20:58891955..59021980hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38130026
hg19130026
hg18130026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067282, nsv1063062
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)dgv4338n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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