A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611720



Internal ID16399129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89464696..89596017hg38UCSC Ensembl
Innerchr8:90476925..90608246hg19UCSC Ensembl
Innerchr8:90546041..90677362hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38131322
hg19131322
hg18131322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117715
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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