A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692719



Internal ID116385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105294300..105311598hg38UCSC Ensembl
chr13:105946651..105963949hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3817299
hg1917299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501358
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692719
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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