A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526454



Internal ID15107061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36143804..36187036hg38UCSC Ensembl
Innerchr22:36539852..36583084hg19UCSC Ensembl
Innerchr22:34869798..34913030hg18UCSC Ensembl
Innerchr22:34864352..34907584hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3843233
hg1943233
hg1843233
hg1743233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702757
Samples
Known GenesAPOL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526454
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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