A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194799



Internal ID20761839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58083940..58089344hg38UCSC Ensembl
chr18:55751172..55756576hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533188
Supporting Variants
Samples
Known GenesNEDD4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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