A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202911



Internal ID20769951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46511601..46516700hg38UCSC Ensembl
chr20:45140240..45145339hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552708
Supporting Variants
Samples
Known GenesZNF334
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00046


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