A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026905



Internal ID85660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100172931..100182818hg38UCSC Ensembl
chr9:102935213..102945100hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389888
hg199888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475557
Supporting Variants
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026905
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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