A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703622



Internal ID127288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91019946..91024220hg38UCSC Ensembl
chr15:91563176..91567450hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384275
hg194275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524293
Supporting Variants
Samples
Known GenesVPS33B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703622
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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