A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270960



Internal ID20838000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54883334..54884500hg38UCSC Ensembl
chr6:54748132..54749298hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568362
Supporting Variants
Samples
Known GenesFAM83B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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