A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937893



Internal ID25976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107391212..107391249hg38UCSC Ensembl
chr3:107110059..107110096hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937893
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.787699


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