A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764890



Internal ID20540750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147183659..147183659hg38UCSC Ensembl
chr5:146563222..146563222hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764890
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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