A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740805



Internal ID20516782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114554188..114561204hg38UCSC Ensembl
chr11:114424910..114431926hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg387017
hg197017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283990
Samples
Known GenesNXPE1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740805
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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