A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026348



Internal ID85306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112762552..112762603hg38UCSC Ensembl
chr9:115524832..115524883hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409834
Supporting Variants
Samples
Known GenesSNX30
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026348
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007493


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