A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957056



Internal ID16251012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38969771..38992223hg38UCSC Ensembl
Innerchr22:39365776..39388228hg19UCSC Ensembl
Innerchr22:37695722..37718174hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3822453
hg1922453
hg1822453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589027
Supporting Variants
Samples
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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