A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028091



Internal ID86424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129510747..129510760hg38UCSC Ensembl
chr9:132273026..132273039hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552759
Supporting Variants
Samples
Known GenesLINC00963
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028091
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007337


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