A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854796



Internal ID22038439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58767050..58767050hg38UCSC Ensembl
chr1:59232722..59232722hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854796
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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