A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484562



Internal ID261972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132317281..132317387hg38UCSC Ensembl
chr7:132002040..132002146hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002648
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484562
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