A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760839



Internal ID20536699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26652249..26652249hg38UCSC Ensembl
chr4:26653871..26653871hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264548
Samples
Known GenesTBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760839
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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