A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv366n223



Internal ID22803334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144076969..144883948hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38806980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6546879, nsv6537837, nsv6536769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv366n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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