A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887541



Internal ID16181497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76699639..76759861hg38UCSC Ensembl
Innerchr18:74411595..74471817hg19UCSC Ensembl
Innerchr18:72540583..72600805hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3860223
hg1960223
hg1860223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577693
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)nssv887541
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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