A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272096



Internal ID20839136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89092233..89094170hg38UCSC Ensembl
chr6:89801952..89803889hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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