A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068855



Internal ID20635895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3860104..3914008hg38UCSC Ensembl
chr20:3840751..3894655hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3853905
hg1953905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527029
Supporting Variants
Samples
Known GenesMAVS, PANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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