A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086032



Internal ID21274058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69358959..69361197hg38UCSC Ensembl
Innerchr8:70271194..70273432hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382239
hg192239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112560
Supporting Variants
Samplessample200
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086032
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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