A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238407



Internal ID20805447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98546428..98546896hg38UCSC Ensembl
chr14:99012765..99013233hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593694
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238407
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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