A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556783



Internal ID21881138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47914742..47914972hg38UCSC Ensembl
chr4:47916759..47916989hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556783
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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