A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759768



Internal ID20535628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123371084..123371084hg38UCSC Ensembl
chr11:123241792..123241792hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759768
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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