A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748733



Internal ID20524760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65825968..65826022hg38UCSC Ensembl
chr11:65593439..65593493hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748733
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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