A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431466



Internal ID21393468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326646..14327080hg38UCSC Ensembl
chr11:14348192..14348626hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753940
SamplesMDQ025
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431466
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer