A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611463



Internal ID16398872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:68832831..68902343hg38UCSC Ensembl
Innerchr8:69745066..69814578hg19UCSC Ensembl
Innerchr8:69907620..69977132hg18UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3869513
hg1969513
hg1869513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156852
SamplesHGDP00950
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611463
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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