A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388841



Internal ID21046394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140518401..140529300hg38UCSC Ensembl
chr4:141439555..141450454hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213054
Samples
Known GenesELMOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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