A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691473



Internal ID115139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84480989..84490721hg38UCSC Ensembl
chr13:85055124..85064856hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg389733
hg199733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507358
Supporting Variants
Samples
Known GenesLINC00333
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691473
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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