A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887326



Internal ID16181282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73056263..73059104hg38UCSC Ensembl
Innerchr18:70723498..70726339hg19UCSC Ensembl
Innerchr18:68874478..68877319hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg382842
hg192842
hg182842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577635
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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