A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859036



Internal ID22042679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109515567..109515567hg38UCSC Ensembl
chr5:108851268..108851268hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244671
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859036
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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