A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701001



Internal ID124667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60023875..60058704hg38UCSC Ensembl
chr15:60316074..60350903hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3834830
hg1934830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701001
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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