A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239191



Internal ID20806231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19630423..19631074hg38UCSC Ensembl
chr16:19641745..19642396hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591350
Supporting Variants
Samples
Known GenesC16orf62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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