A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858599



Internal ID22042242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152721314..152721314hg38UCSC Ensembl
chr5:152100874..152100874hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858599
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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