A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705113



Internal ID128779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90283567..90313247hg38UCSC Ensembl
chr15:90826799..90856479hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3829681
hg1929681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705113
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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