A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216643



Internal ID20783683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152960201..153019400hg38UCSC Ensembl
chr6:153281336..153340535hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3859200
hg1959200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606117
Supporting Variants
Samples
Known GenesFBXO5, MTRF1L, RGS17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216643
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00081


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