A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1118317



Internal ID15624817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:109750684..109809367hg38UCSC Ensembl
Innerchr8:110762913..110821596hg19UCSC Ensembl
Innerchr8:110832089..110890772hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3858684
hg1958684
hg1858684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611880
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)nssv1118317
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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