A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899369



Internal ID352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20606079..20607344hg38UCSC Ensembl
chr1:20932572..20933837hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416280
Supporting Variants
Samples
Known GenesCDA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899369
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00359


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