A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436018



Internal ID214645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180960358..180961360hg38UCSC Ensembl
chr3:180678146..180679148hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944680
Samples
Known GenesFXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436018
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