A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703937



Internal ID127603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68988321..68996652hg38UCSC Ensembl
chr15:69280660..69288991hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388332
hg198332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518711
Supporting Variants
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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