A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106859



Internal ID15960045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15458586..15491106hg38UCSC Ensembl
Innerchr8:15316095..15348615hg19UCSC Ensembl
Innerchr8:15360466..15392986hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3832521
hg1932521
hg1832521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610526
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)nssv1106859
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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