A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748444



Internal ID20524469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129744508..129744640hg38UCSC Ensembl
chr11:129614403..129614535hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748444
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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