A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027482



Internal ID86029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95626004..95626346hg38UCSC Ensembl
chr9:98388286..98388628hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027482
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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