A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219176



Internal ID20786216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39110905..39111437hg38UCSC Ensembl
chr14:39580109..39580641hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219176
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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