A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763495



Internal ID20539355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119982228..119982228hg38UCSC Ensembl
chr11:119852937..119852937hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763495
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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