A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376497



Internal ID21034050
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 StatusM
Merged Variants
Supporting Variantsnssv18209524
Samples
Known GenesELOVL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376497
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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