A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766204



Internal ID20542064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88473683..88473683hg38UCSC Ensembl
chr13:89125938..89125938hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766204
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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