A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2696n223



Internal ID22805664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14685369..14685815hg38UCSC Ensembl
chr16:14779226..14779672hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584072, nsv6589433
Samples
Known GenesPLA2G10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2696n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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