A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699875



Internal ID123541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23798081..23804386hg38UCSC Ensembl
chr15:24043228..24049533hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386306
hg196306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494583
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699875
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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