A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724914



Internal ID148580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60761980..60772000hg38UCSC Ensembl
chr17:58839341..58849361hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3810021
hg1910021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531539
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724914
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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