A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750540



Internal ID20526496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91709289..91709289hg38UCSC Ensembl
chr5:91005106..91005106hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385913
hg195913
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750540
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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