A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv492n21



Internal ID22766684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104529720..104531740hg38UCSC Ensembl
chr9:107292001..107294021hg19UCSC Ensembl
chr9:106331822..106333842hg18UCSC Ensembl
chr9:104371556..104373576hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382021
hg192021
hg182021
hg172021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527377, nsv527720
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv492n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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