A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746314



Internal ID20522326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19376551..19385728hg38UCSC Ensembl
chr2:19576312..19585489hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg389178
hg199178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746314
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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