A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738508



Internal ID162174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96350297..96350362hg38UCSC Ensembl
chr9:99112579..99112644hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493000
Supporting Variants
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738508
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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