A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701678



Internal ID125344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45614004..45617342hg38UCSC Ensembl
chr15:45906202..45909540hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383339
hg193339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701678
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer