A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223251



Internal ID20790291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19749605..19749984hg38UCSC Ensembl
chr14:20217764..20218143hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223251
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00034


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