A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518711



Internal ID295081
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 StatusM
Merged Variants
Supporting Variantsnssv17703937
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518711
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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