A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2036n223



Internal ID22805004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20465877..20466454hg38UCSC Ensembl
chr14:20934036..20934613hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577821, nsv6585461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2036n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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