A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493408



Internal ID270592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44960893..44966266hg38UCSC Ensembl
chr10:45456341..45461714hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385374
hg195374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032814
Samples
Known GenesRASSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493408
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