A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762614



Internal ID20538474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118331100..118331100hg38UCSC Ensembl
chr11:118201815..118201815hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762614
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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