A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686077



Internal ID109743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22229957..22230010hg38UCSC Ensembl
chr13:22804096..22804149hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513349
Supporting Variants
Samples
Known GenesLINC00540
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686077
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.025601


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