A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6449n223



Internal ID22809417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149669088..149669955hg38UCSC Ensembl
chr6:149990224..149991091hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6556000, nsv6574132
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6449n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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