A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7557n54



Internal ID22775452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32583046..32585304hg38UCSC Ensembl
chr20:31170848..31173106hg19UCSC Ensembl
chr20:30634509..30636767hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382259
hg192259
hg182259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585915, nsv585916
Samples
Known GenesC20orf112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7557n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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