A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186282



Internal ID20753323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26623861..26624334hg38UCSC Ensembl
chr13:27197998..27198471hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483575
Supporting Variants
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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