A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178545



Internal ID20745585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94641867..94647043hg38UCSC Ensembl
chr11:94375033..94380209hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385177
hg195177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00135


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