A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6413n223



Internal ID22809381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134536623..134537846hg38UCSC Ensembl
chr6:134857761..134858984hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6563154, nsv6568633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6413n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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