A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100160



Internal ID22009393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120083055..120083055hg38UCSC Ensembl
chr11:119953764..119953764hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100160
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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