A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576106



Internal ID20949177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68210199..68211162hg38UCSC Ensembl
chr16:68244102..68245065hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243644
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576106
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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