A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688152



Internal ID111818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58273734..58285863hg38UCSC Ensembl
chr13:58847868..58859997hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3812130
hg1912130
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688152
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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