A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878874



Internal ID16172830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29851705..29922765hg38UCSC Ensembl
Innerchr18:27431670..27502730hg19UCSC Ensembl
Innerchr18:25685668..25756728hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3871061
hg1971061
hg1871061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576601
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)nssv878874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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