A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586679



Internal ID18538274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23943610..23995743hg38UCSC Ensembl
Innerchr22:24285797..24337937hg19UCSC Ensembl
Innerchr22:22615797..22667937hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3852134
hg1952141
hg1852141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065549
Supporting Variants
Samples
Known GenesDDT, DDTL, GSTT2, GSTT2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586679
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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