A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766459



Internal ID20542319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139726632..139726632hg38UCSC Ensembl
chr4:140647786..140647786hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263234
Samples
Known GenesMAML3, MGST2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766459
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer