A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237718



Internal ID20804758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92139371..92139851hg38UCSC Ensembl
chr14:92605715..92606195hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591915
Supporting Variants
Samples
Known GenesCPSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237718
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00044


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