A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243643



Internal ID20810684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68196581..68197214hg38UCSC Ensembl
chr16:68230484..68231117hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588631
Supporting Variants
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243643
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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