A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv446n21



Internal ID22766638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9086797..9124886hg38UCSC Ensembl
chr8:8944307..8982396hg19UCSC Ensembl
chr8:8981717..9019806hg18UCSC Ensembl
chr8:8981717..9019806hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3838090
hg1938090
hg1838090
hg1738090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526092, nsv523098
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv446n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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