A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580843



Internal ID20953914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80422986..80424127hg38UCSC Ensembl
chr14:80889329..80890470hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381142
hg191142
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238194
Samples
Known GenesDIO2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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