A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3734202



Internal ID18685797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33397437..33427322hg38UCSC Ensembl
Innerchr22:33793423..33823308hg19UCSC Ensembl
Innerchr22:32123423..32153308hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3829886
hg1929886
hg1829886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058261
Supporting Variants
Samples
Known GenesLARGE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3734202
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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