A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194137



Internal ID20761177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79844601..79883700hg38UCSC Ensembl
chr13:80418736..80457835hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3839100
hg1939100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194137
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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