A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588951



Internal ID16029674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36140981..36187036hg38UCSC Ensembl
Innerchr22:36537029..36583084hg19UCSC Ensembl
Innerchr22:34866975..34913030hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3846056
hg1946056
hg1846056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8093n54
Supporting Variantsnssv955462
Samples
Known GenesAPOL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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