A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184312



Internal ID20751352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36155902..36156997hg38UCSC Ensembl
chr18:33735865..33736960hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517774
Supporting Variants
Samples
Known GenesELP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184312
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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