A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267814



Internal ID20834854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109418728..109419700hg38UCSC Ensembl
chr6:109739931..109740903hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563725
Supporting Variants
Samples
Known GenesPPIL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267814
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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