A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213616



Internal ID20780656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40565996..40602034hg38UCSC Ensembl
chr4:40568013..40604051hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3836039
hg1936039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383715
Supporting Variants
Samples
Known GenesRBM47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213616
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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