A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899794



Internal ID645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17157604..17188087hg38UCSC Ensembl
chr1:17484099..17514582hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3830484
hg1930484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419077
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899794
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004372


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