A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854183



Internal ID22037826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116025573..116025573hg38UCSC Ensembl
chr3:115744420..115744420hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254569
Supporting Variants
Samples
Known GenesLSAMP
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854183
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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