A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024986



Internal ID84388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91298968..91302267hg38UCSC Ensembl
chr9:94061250..94064549hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487347
Supporting Variants
Samples
Known GenesAUH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024986
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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