A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753945



Internal ID20529805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63092523..63092523hg38UCSC Ensembl
chr11:62859995..62859995hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281262
Samples
Known GenesSLC22A24
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753945
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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