A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv470n21



Internal ID22766662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110101478..110132390hg38UCSC Ensembl
chr8:111113707..111144619hg19UCSC Ensembl
chr8:111182883..111213795hg18UCSC Ensembl
chr8:111182883..111213795hg17UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3830913
hg1930913
hg1830913
hg1730913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522041, nsv526118
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv470n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer