A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743881



Internal ID20519873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221920223..221920278hg38UCSC Ensembl
chr1:222093565..222093620hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743881
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