A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026100



Internal ID85133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88998340..88999785hg38UCSC Ensembl
chr9:91613255..91614700hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491340
Supporting Variants
Samples
Known GenesS1PR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026100
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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