A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190721



Internal ID20757761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39356145..39359476hg38UCSC Ensembl
chr17:37512398..37515729hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383332
hg193332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501307
Supporting Variants
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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