A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179721



Internal ID20746761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18951795..18953816hg38UCSC Ensembl
chr13:19525935..19527956hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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