A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767392



Internal ID20543252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46161853..46161853hg38UCSC Ensembl
chr11:46183404..46183404hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767392
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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