A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431444



Internal ID21393446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128467106..128526105hg38UCSC Ensembl
chr11:128337001..128396000hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3859000
hg1959000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15745791
SamplesSMI041
Known GenesETS1, MIR6090
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431444
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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