A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7567n54



Internal ID22775462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38377270..38386275hg38UCSC Ensembl
chr20:37005912..37014917hg19UCSC Ensembl
chr20:36439326..36448331hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg389006
hg199006
hg189006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585965, nsv585966
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7567n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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