A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004958



Internal ID22066589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73648641..73762011hg38UCSC Ensembl
Outerchr8:73643047..73763015hg38UCSC Ensembl
Innerchr8:74560876..74674246hg19UCSC Ensembl
Outerchr8:74555282..74675250hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38119969
hg19119969
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154367
Supporting Variants
Samples
Known GenesSTAU2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004958
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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