A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2890n223



Internal ID22805858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56626578..56633900hg38UCSC Ensembl
chr16:56660490..56667812hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg387323
hg197323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6507806, nsv6512340
Samples
Known GenesMT1E, MT1M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2890n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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