A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986599



Internal ID20553639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109928100..109928743hg38UCSC Ensembl
chr11:109798826..109799469hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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