A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740620



Internal ID20516596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43046816..43046882hg38UCSC Ensembl
chr2:43273955..43274021hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740620
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