A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704262



Internal ID127928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65300798..65300918hg38UCSC Ensembl
chr15:65593136..65593256hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518911
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704262
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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