A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686026



Internal ID109692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21245003..21324278hg38UCSC Ensembl
chr13:21819142..21898417hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3879276
hg1979276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505583
Supporting Variants
Samples
Known GenesLINC00539, MIPEPP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686026
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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