A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6176n223



Internal ID22809144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43407311..43407973hg38UCSC Ensembl
chr6:43375049..43375711hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6560254, nsv6563138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6176n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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