A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764118



Internal ID20539978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112210088..112210088hg38UCSC Ensembl
chr13:112864402..112864402hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764118
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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