A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750918



Internal ID20526778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87632899..87632899hg38UCSC Ensembl
chr5:86928716..86928716hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750918
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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