A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911553



Internal ID8470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:40284453..40319330hg38UCSC Ensembl
chr2:40511593..40546470hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3834878
hg1934878
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561542
Supporting Variants
Samples
Known GenesSLC8A1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911553
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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