A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16918537



Internal ID13127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101049676..101049848hg38UCSC Ensembl
chr2:101666138..101666310hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449954
Supporting Variants
Samples
Known GenesTBC1D8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16918537
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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