A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5471636



Internal ID249366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170810389..170815801hg38UCSC Ensembl
chr4:171731540..171736952hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg385413
hg195413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5471636
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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