A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465083



Internal ID21122636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117833481..117835004hg38UCSC Ensembl
chr11:117704196..117705719hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987170
Samples
Known GenesFXYD6-FXYD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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