A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473333



Internal ID21130886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117552092..117552336hg38UCSC Ensembl
chr11:117422807..117423051hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987161
Samples
Known GenesDSCAML1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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