A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239284



Internal ID20806325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55712067..55726721hg38UCSC Ensembl
chr16:55745979..55760633hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3814655
hg1914655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580048
Supporting Variants
Samples
Known GenesCES1P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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