A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203266



Internal ID20770306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3191107..3407325hg38UCSC Ensembl
chr20:3171753..3387972hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38216219
hg19216220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529546
Supporting Variants
Samples
Known GenesC20orf194, DDRGK1, ITPA, SLC4A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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