A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890330



Internal ID167717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151762500..151762989hg38UCSC Ensembl
chr1:151734976..151735465hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427787
Supporting Variants
Samples
Known GenesMRPL9, OAZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890330
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