A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555589



Internal ID20928674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138728529..138729155hg38UCSC Ensembl
chr6:139049666..139050292hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272468
Samples
Known GenesLOC100507462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555589
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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