A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209524



Internal ID20776564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110141322..110158920hg38UCSC Ensembl
chr4:111062478..111080076hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3817599
hg1917599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376497
Supporting Variants
Samples
Known GenesELOVL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209524
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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