A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184287



Internal ID20751327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43415856..43416378hg38UCSC Ensembl
chr13:43989992..43990514hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475917
Supporting Variants
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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