A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474936



Internal ID21132489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120321739..120328179hg38UCSC Ensembl
chr11:120192448..120198888hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386441
hg196441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987253
Samples
Known GenesTMEM136
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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