A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6366n223



Internal ID22809334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110880693..110881821hg38UCSC Ensembl
chr6:111201896..111203024hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6571166, nsv6556635
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6366n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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