A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859059



Internal ID22042702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112670869..112670869hg38UCSC Ensembl
chr5:112006566..112006566hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244694
Supporting Variants
Samples
Known GenesLOC102467216
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859059
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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