A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533775



Internal ID309655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60917726..60922260hg38UCSC Ensembl
chr17:58995087..58999621hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg384535
hg194535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724926
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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