A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686904



Internal ID110570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36628920..36630910hg38UCSC Ensembl
chr13:37203057..37205047hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686904
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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