A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699823



Internal ID123489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55801533..55807469hg38UCSC Ensembl
chr15:56093731..56099667hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385937
hg195937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699823
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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