A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848692



Internal ID22032335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80270144..80270144hg38UCSC Ensembl
chr15:80562486..80562486hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249859
Supporting Variants
Samples
Known GenesLINC00927
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848692
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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