A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2721n223



Internal ID22805689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19538553..19539071hg38UCSC Ensembl
chr16:19549875..19550393hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6576457, nsv6582241
Samples
Known GenesCCP110
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2721n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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