A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555598



Internal ID20928683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110968489..110969052hg38UCSC Ensembl
chr6:111289692..111290255hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555598
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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