A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203233



Internal ID20770273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23403332..23414052hg38UCSC Ensembl
chr20:23383969..23394689hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3810721
hg1910721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521336
Supporting Variants
Samples
Known GenesNAPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203233
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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