A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216642



Internal ID20783682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152956201..153022300hg38UCSC Ensembl
chr6:153277336..153343435hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3866100
hg1966100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607244
Supporting Variants
Samples
Known GenesFBXO5, MTRF1L, RGS17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0011


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