A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6057n223



Internal ID22809025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11125083..11126303hg38UCSC Ensembl
chr6:11125316..11126536hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6561594, nsv6562375
Samples
Known GenesSMIM13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6057n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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