A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205276



Internal ID20772316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50797719..50808051hg38UCSC Ensembl
chr20:49414256..49424588hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3810333
hg1910333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554533
Supporting Variants
Samples
Known GenesBCAS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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