A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588952



Internal ID16029675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36143804..36187036hg38UCSC Ensembl
Innerchr22:36539852..36583084hg19UCSC Ensembl
Innerchr22:34869798..34913030hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3843233
hg1943233
hg1843233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8093n54
Supporting Variantsnssv955463
Samples
Known GenesAPOL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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