A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239931



Internal ID20806971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14464561..14465126hg38UCSC Ensembl
chr16:14558418..14558983hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578012
Supporting Variants
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239931
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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