A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703673



Internal ID127339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92172766..92175320hg38UCSC Ensembl
chr15:92715996..92718550hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382555
hg192555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703673
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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