A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028543



Internal ID86725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121315497..121315618hg38UCSC Ensembl
chr9:124077775..124077896hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488319
Supporting Variants
Samples
Known GenesGSN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028543
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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