A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267798



Internal ID20834838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108753988..108754988hg38UCSC Ensembl
chr6:109075191..109076191hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568513
Supporting Variants
Samples
Known GenesLINC00222
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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