A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv244n21



Internal ID22766436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16256192..16267808hg38UCSC Ensembl
chr20:16236837..16248453hg19UCSC Ensembl
chr20:16184837..16196453hg18UCSC Ensembl
chr20:16184837..16196453hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3811617
hg1911617
hg1811617
hg1711617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516591, nsv519621
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv244n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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