A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190491



Internal ID20757531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107867701..107872700hg38UCSC Ensembl
chr13:108520049..108525048hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00061


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