A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473731



Internal ID251414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97653930..97809420hg38UCSC Ensembl
chr4:98575081..98730571hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38155491
hg19155491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954209
Samples
Known GenesSTPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473731
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