A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908054



Internal ID6157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110678567..110686463hg38UCSC Ensembl
chr1:111221189..111229085hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg387897
hg197897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428487
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908054
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