A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv466n21



Internal ID20132187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101828803..101881398hg38UCSC Ensembl
chr8:102841031..102893626hg19UCSC Ensembl
chr8:102910207..102962802hg18UCSC Ensembl
chr8:102910207..102962802hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3852596
hg1952596
hg1852596
hg1752596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518162, nsv523850
Samples
Known GenesNCALD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv466n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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