A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022890



Internal ID82960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38395054..38395094hg38UCSC Ensembl
chr9:38395051..38395091hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539304
Supporting Variants
Samples
Known GenesALDH1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022890
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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