A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704116



Internal ID127782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89416275..89418417hg38UCSC Ensembl
chr15:89959506..89961648hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382143
hg192143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526251
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704116
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004527


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