A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219737



Internal ID20786777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52425186..52426896hg38UCSC Ensembl
chr14:52891904..52893614hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219737
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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