A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7507n54



Internal ID22775402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16586557..16608358hg38UCSC Ensembl
chr20:16567202..16589003hg19UCSC Ensembl
chr20:16515202..16537003hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3821802
hg1921802
hg1821802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585653, nsv585652, nsv585654, nsv585651
SamplesHGDP00912, HGDP00904, HGDP00934, HGDP00942, HGDP00921, HGDP00920
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7507n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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