A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692598



Internal ID116264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99577875..99580576hg38UCSC Ensembl
chr13:100230129..100232830hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692598
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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