A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610774



Internal ID16051497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23071837..23165107hg38UCSC Ensembl
Innerchr8:22929350..23022620hg19UCSC Ensembl
Innerchr8:22985295..23078565hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3893271
hg1993271
hg1893271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12057n54
Supporting Variantsnssv1107478
Samples
Known GenesLOC254896, LOC286059, TNFRSF10C, TNFRSF10D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610774
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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