A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580394



Internal ID21772437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140099149..140099241hg38UCSC Ensembl
chr8:141109248..141109340hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019622
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580394
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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