A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173375



Internal ID20740415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106977212..106979771hg38UCSC Ensembl
chr9:109739493..109742052hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382560
hg192560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445918
Supporting Variants
Samples
Known GenesMIR548Q, ZNF462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01259


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