A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732422



Internal ID20508346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154666552..154668759hg38UCSC Ensembl
chr1:154639028..154641235hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382208
hg192208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732422
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