A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023985



Internal ID83702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88567018..88567024hg38UCSC Ensembl
chr9:91181933..91181939hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552721
Supporting Variants
Samples
Known GenesNXNL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023985
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.037592


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