A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6882n223



Internal ID22809850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66179261..66181364hg38UCSC Ensembl
chr7:65644248..65646351hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382104
hg192104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6573922, nsv6555877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6882n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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