A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2880n223



Internal ID22805848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52020401..52100800hg38UCSC Ensembl
chr16:52054313..52134712hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3880400
hg1980400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6497796, nsv6508646
Samples
Known GenesC16orf97, LINC00919, LOC102467079
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2880n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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