A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521684



Internal ID20895045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46227671..46234289hg38UCSC Ensembl
chr18:43807637..43814255hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg386619
hg196619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185408
Samples
Known GenesC18orf25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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