A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841000



Internal ID22024643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28083233..28083233hg38UCSC Ensembl
chr9:28083231..28083231hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247008
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841000
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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