A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887258



Internal ID16181214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71675679..71872032hg38UCSC Ensembl
Innerchr18:69342915..69539268hg19UCSC Ensembl
Innerchr18:67493895..67690248hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38196354
hg19196354
hg18196354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577596
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)nssv887258
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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