A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219110



Internal ID20786150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31238334..31238903hg38UCSC Ensembl
chr14:31707540..31708109hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219110
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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