A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764947



Internal ID20540807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121427665..121427665hg38UCSC Ensembl
chr11:121298374..121298374hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764947
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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