A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858868



Internal ID22042511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171757016..171757016hg38UCSC Ensembl
chr5:171184020..171184020hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858868
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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