A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760904



Internal ID20536764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85592308..85592308hg38UCSC Ensembl
chr13:86166443..86166443hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760904
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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