A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280306



Internal ID20847346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19274357..19287111hg38UCSC Ensembl
chr9:19274355..19287109hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3812755
hg1912755
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574927
Supporting Variants
Samples
Known GenesDENND4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280306
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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