A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717072



Internal ID140738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31486086..31486137hg38UCSC Ensembl
chr18:29066049..29066100hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717072
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01202


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