A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561388



Internal ID20934459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83716385..83717048hg38UCSC Ensembl
chr6:84426104..84426767hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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