A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741511



Internal ID20517488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64270932..64271004hg38UCSC Ensembl
chr11:64038404..64038476hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280021
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741511
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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