A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702657



Internal ID126323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46438106..46438887hg38UCSC Ensembl
chr15:46730304..46731085hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003122


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