A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203314



Internal ID20770354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3543154..3905714hg38UCSC Ensembl
chr20:3523801..3886361hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38362561
hg19362561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533157
Supporting Variants
Samples
Known GenesADAM33, AP5S1, ATRN, C20orf27, CDC25B, CENPB, GFRA4, HSPA12B, MAVS, PANK2, SIGLEC1, SPEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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