A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239221



Internal ID20806262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20803872..20804393hg38UCSC Ensembl
chr16:20815194..20815715hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577657
Supporting Variants
Samples
Known GenesERI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239221
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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