A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025866



Internal ID84981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96349648..96353417hg38UCSC Ensembl
chr9:99111930..99115699hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg383770
hg193770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486035
Supporting Variants
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025866
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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