A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2662n223



Internal ID22805630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3572999..3574037hg38UCSC Ensembl
chr16:3623000..3624038hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6581132, nsv6576649
Samples
Known GenesNLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2662n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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