A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703927



Internal ID127593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68792880..68793770hg38UCSC Ensembl
chr15:69085219..69086109hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521359
Supporting Variants
Samples
Known GenesANP32A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703927
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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