A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240716



Internal ID20807756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53180810..53182073hg38UCSC Ensembl
chr16:53214722..53215985hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592584
Supporting Variants
Samples
Known GenesCHD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240716
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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