A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692491



Internal ID116157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85787429..85787429hg38UCSC Ensembl
chr13:86361564..86361564hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692491
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.333066


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