A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517806



Internal ID294214
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 StatusM
Merged Variants
Supporting Variantsnssv17713804
Samples
Known GenesBZRAP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517806
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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