A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760079



Internal ID20535939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94997037..94997037hg38UCSC Ensembl
chr13:95649291..95649291hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760079
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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