A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213589



Internal ID20780629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39751312..39814980hg38UCSC Ensembl
chr4:39752932..39816600hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3863669
hg1963669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381801
Supporting Variants
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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