A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957061



Internal ID16251017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38982647..38990107hg38UCSC Ensembl
Innerchr22:39378652..39386112hg19UCSC Ensembl
Innerchr22:37708598..37716058hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387461
hg197461
hg187461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589030
Supporting Variants
Samples
Known GenesAPOBEC3A_B, APOBEC3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957061
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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