A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737337



Internal ID19035618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967602..38999281hg38UCSC Ensembl
Innerchr22:39363607..39395286hg19UCSC Ensembl
Innerchr22:37693553..37725232hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3831680
hg1931680
hg1831680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061959
Supporting Variants
Samples
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3737337
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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