A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754722



Internal ID20530582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110244316..110244316hg38UCSC Ensembl
chr9:113006596..113006596hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265944
Samples
Known GenesTXN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754722
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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