A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760853



Internal ID20536713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95322047..95322047hg38UCSC Ensembl
chr11:95055211..95055211hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760853
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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