A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841485



Internal ID22025128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77341499..77341499hg38UCSC Ensembl
chr9:79956415..79956415hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257788
Supporting Variants
Samples
Known GenesVPS13A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841485
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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