A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909949



Internal ID7409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9884839..9884891hg38UCSC Ensembl
chr2:10024968..10025020hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446000
Supporting Variants
Samples
Known GenesTAF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909949
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