A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687611



Internal ID111277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48947592..48947643hg38UCSC Ensembl
chr13:49521728..49521779hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg382569
hg192569
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559582
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687611
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.056518


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