A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611566



Internal ID16398975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77214090..77333299hg38UCSC Ensembl
Innerchr8:78126326..78245535hg19UCSC Ensembl
Innerchr8:78288881..78408090hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38119210
hg19119210
hg18119210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117007
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611566
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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