A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180107



Internal ID20747147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42471501..42479100hg38UCSC Ensembl
chr13:43045637..43053236hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180107
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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