A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1119663



Internal ID15972849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:113840898..113895173hg38UCSC Ensembl
Innerchr8:114853127..114907402hg19UCSC Ensembl
Innerchr8:114922303..114976578hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3854276
hg1954276
hg1854276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611958
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)nssv1119663
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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