A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902266



Internal ID2310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19959971..19962076hg38UCSC Ensembl
chr1:20286464..20288569hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902266
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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