A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703926



Internal ID127592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68792137..68792287hg38UCSC Ensembl
chr15:69084476..69084626hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530432
Supporting Variants
Samples
Known GenesANP32A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703926
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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