A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238399



Internal ID20805439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96518464..96518976hg38UCSC Ensembl
chr14:96984801..96985313hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576282
Supporting Variants
Samples
Known GenesPAPOLA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238399
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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