A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558736



Internal ID20931807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85474379..85477336hg38UCSC Ensembl
chr6:86184097..86187054hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg382958
hg192958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274819
Samples
Known GenesNT5E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558736
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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