A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611978



Internal ID16399387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114433176..114492205hg38UCSC Ensembl
Innerchr8:115445405..115504434hg19UCSC Ensembl
Innerchr8:115514581..115573610hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3859030
hg1959030
hg1859030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12279n54
Supporting Variantsnssv1119766
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611978
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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