A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018383



Internal ID79886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142648080..142657748hg38UCSC Ensembl
chr8:143729464..143739162hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg389669
hg199699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491002
Supporting Variants
Samples
Known GenesJRK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018383
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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