A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714236



Internal ID137902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68729024..68731154hg38UCSC Ensembl
chr17:66725165..66727295hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382131
hg192131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714236
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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