A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213023



Internal ID20780063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138552001..138560800hg38UCSC Ensembl
chr4:139473155..139481954hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00109


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