A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914632



Internal ID10501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67419015..67419015hg38UCSC Ensembl
chr2:67646147..67646147hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914632
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000157


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