A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686656



Internal ID110322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31452411..31452577hg38UCSC Ensembl
chr13:32026548..32026714hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686656
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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