A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741146



Internal ID20517123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60329926..60330440hg38UCSC Ensembl
chr11:60097399..60097913hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741146
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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