A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186549



Internal ID20753589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12171601..12442300hg38UCSC Ensembl
chr18:12171600..12442299hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38270700
hg19270700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533223
Supporting Variants
Samples
Known GenesAFG3L2, C18orf61, CIDEA, SLMO1, TUBB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186549
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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