A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764921



Internal ID20540781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86731536..86731536hg38UCSC Ensembl
chr11:86442578..86442578hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764921
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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