A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567117



Internal ID20940188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138754395..138756435hg38UCSC Ensembl
chr6:139075532..139077572hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg382041
hg192041
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272470
Samples
Known GenesLOC100507462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567117
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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