A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713804



Internal ID137470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58329793..58329971hg38UCSC Ensembl
chr17:56407154..56407332hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517806
Supporting Variants
Samples
Known GenesBZRAP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713804
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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