A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221160



Internal ID20788200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129762850..129817423hg38UCSC Ensembl
chr9:132525129..132579702hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3854574
hg1954574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438335
Supporting Variants
Samples
Known GenesTOR1A, TOR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221160
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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