A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2035n223



Internal ID22805003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20453354..20454037hg38UCSC Ensembl
chr14:20921513..20922196hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584621, nsv6578323
Samples
Known GenesOSGEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2035n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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