A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025955



Internal ID85037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77331938..77331989hg38UCSC Ensembl
chr9:79946854..79946905hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5400509
Supporting Variants
Samples
Known GenesVPS13A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025955
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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