A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926074



Internal ID18122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223078271..223078440hg38UCSC Ensembl
chr2:223942989..223943158hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926074
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.043709


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