A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849359



Internal ID22033002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44677452..44677452hg38UCSC Ensembl
chr18:42257417..42257417hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849359
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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