A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212886



Internal ID20779926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32732393..32748550hg38UCSC Ensembl
chr4:32734015..32750172hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3816158
hg1916158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00066


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