A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733455



Internal ID20509385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128414443..128414506hg38UCSC Ensembl
chr11:128284338..128284401hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733455
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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