A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390073



Internal ID21381208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126290631..126292840hg38UCSC Ensembl
chr11:126160526..126162735hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382210
hg192210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705251
Samples
Known GenesTIRAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390073
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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