A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1119668



Internal ID15972854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114056622..114172435hg38UCSC Ensembl
Innerchr8:115068851..115184664hg19UCSC Ensembl
Innerchr8:115138027..115253840hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38115814
hg19115814
hg18115814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611963
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)nssv1119668
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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