A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757362



Internal ID20533222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92406131..92406131hg38UCSC Ensembl
chr11:92139297..92139297hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287296
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757362
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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