A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915736



Internal ID22690954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117707882..117707964hg38UCSC Ensembl
chr9:120470160..120470242hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436569
Samples
Known GenesTLR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915736
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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