A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150621



Internal ID15878580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70658460..71275327hg38UCSC Ensembl
Innerchr18:68325696..68942563hg19UCSC Ensembl
Innerchr18:66476676..67093543hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38616868
hg19616868
hg18616868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577581
Supporting Variants
SamplesHGDP01228
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150621
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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