A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518532



Internal ID20891893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55659601..55670700hg38UCSC Ensembl
chr18:53326832..53337931hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3811100
hg1911100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518532
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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