A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686821



Internal ID110487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34867117..34868364hg38UCSC Ensembl
chr13:35441254..35442501hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512745
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686821
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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