A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687222



Internal ID110888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42457883..42511668hg38UCSC Ensembl
chr13:43032019..43085804hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3853786
hg1953786
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555969
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687222
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.296597


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