A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762481



Internal ID20538341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18560125..18560125hg38UCSC Ensembl
chr11:18581672..18581672hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263367
Samples
Known GenesUEVLD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762481
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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