A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877334



Internal ID16171290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1753952..1872420hg38UCSC Ensembl
Innerchr18:1753953..1872421hg19UCSC Ensembl
Innerchr18:1743953..1862421hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38118469
hg19118469
hg18118469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576274
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)nssv877334
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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