A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686980



Internal ID110646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38076923..38077026hg38UCSC Ensembl
chr13:38651060..38651163hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497513
Supporting Variants
Samples
Known GenesLINC00571
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686980
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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