A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914911



Internal ID10698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61521170..61521197hg38UCSC Ensembl
chr2:61748305..61748332hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556195
Supporting Variants
Samples
Known GenesXPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914911
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