A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612980



Internal ID16400389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:145025976..145068028hg38UCSC Ensembl
Innerchr8:146251362..146293414hg19UCSC Ensembl
Innerchr8:146222166..146264218hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3842053
hg1942053
hg1842053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1125839
Samples
Known GenesC8orf33
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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