A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567666



Internal ID20940737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108297287..108299267hg38UCSC Ensembl
chr6:108618491..108620471hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267783
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567666
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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