A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238571



Internal ID20805611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70231133..70470238hg38UCSC Ensembl
chr14:70697850..70936955hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38239106
hg19239106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595416
Supporting Variants
Samples
Known GenesADAM20P1, ADAM21, ADAM21P1, COX16, SYNJ2BP, SYNJ2BP-COX16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238571
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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