A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472293



Internal ID21129846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126361950..126377553hg38UCSC Ensembl
chr11:126231845..126247448hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3815604
hg1915604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987339
Samples
Known GenesST3GAL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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