A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191269



Internal ID20758309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26558001..26561300hg38UCSC Ensembl
chr13:27132138..27135437hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487831
Supporting Variants
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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