A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759826



Internal ID20535686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53052872..53052872hg38UCSC Ensembl
chr15:53345069..53345069hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759826
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