A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611668



Internal ID16399077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85644902..85661840hg38UCSC Ensembl
Innerchr8:86557131..86574069hg19UCSC Ensembl
Innerchr8:86744383..86761321hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3816939
hg1916939
hg1816939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117432
Samples
Known GenesREXO1L1, REXO1L2P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611668
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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