A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027293



Internal ID85914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128165859..128179900hg38UCSC Ensembl
chr9:130928138..130942179hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3814042
hg1914042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490088
Supporting Variants
Samples
Known GenesCIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027293
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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