A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894926



Internal ID170790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203821404..203824327hg38UCSC Ensembl
chr1:203790532..203793455hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382924
hg192924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438441
Supporting Variants
Samples
Known GenesZC3H11A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894926
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