A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085191



Internal ID21269715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72244272..72253885hg38UCSC Ensembl
Innerchr8:73156507..73166120hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg389614
hg199614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118114
Supporting Variants
Samplessample142
Known GenesLOC392232
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085191
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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