A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017533



Internal ID79338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122201651..122545984hg38UCSC Ensembl
chr8:123213890..123558223hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38344334
hg19344334
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017533
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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