A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516883



Internal ID20890244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50862869..50863279hg38UCSC Ensembl
chr18:48389239..48389649hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516883
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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