A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409907



Internal ID189227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185863677..185863714hg38UCSC Ensembl
chr4:186784831..186784868hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735244
Samples
Known GenesSORBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409907
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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