A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2076n223



Internal ID22805044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24386037..24386586hg38UCSC Ensembl
chr14:24855243..24855792hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6578078, nsv6576831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2076n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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