A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440432



Internal ID218939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234023009..234034992hg38UCSC Ensembl
chr1:234158755..234170738hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3811984
hg1911984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897933
Samples
Known GenesSLC35F3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440432
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