A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438569



Internal ID21096122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117433585..117758794hg38UCSC Ensembl
chr9:120195863..120521072hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38325210
hg19325210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226943
Samples
Known GenesTLR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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