A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519526



Internal ID20892887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33518108..34009759hg38UCSC Ensembl
chr18:31098072..31589723hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38491652
hg19491652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188826
Samples
Known GenesASXL3, NOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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