A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731551



Internal ID20507471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183067214..183067403hg38UCSC Ensembl
chr2:183931942..183932131hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731551
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