A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1120445



Internal ID15973631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:120841165..121173175hg38UCSC Ensembl
Innerchr8:121853405..122185415hg19UCSC Ensembl
Innerchr8:121922586..122254596hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38332011
hg19332011
hg18332011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612114
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)nssv1120445
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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