A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610866



Internal ID16051589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27526384..27593018hg38UCSC Ensembl
Innerchr8:27383901..27450535hg19UCSC Ensembl
Innerchr8:27439818..27506452hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3866635
hg1966635
hg1866635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109355
Samples
Known GenesEPHX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610866
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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