A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1114110



Internal ID15967296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45927486..45975113hg38UCSC Ensembl
Innerchr8:46839108..46886735hg19UCSC Ensembl
Innerchr8:46958273..47005900hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3847628
hg1947628
hg1847628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611222
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)nssv1114110
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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