A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181679



Internal ID20748719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96587601..96593500hg38UCSC Ensembl
chr11:96458601..96464500hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468385
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181679
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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