A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3562968



Internal ID18861249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71301821..71382241hg38UCSC Ensembl
Innerchr18:68969057..69049477hg19UCSC Ensembl
Innerchr18:67120037..67200457hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3880421
hg1980421
hg1880421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056964
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3562968
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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