A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2943n223



Internal ID22805911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77983730..78060495hg38UCSC Ensembl
chr16:78017627..78094392hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3876766
hg1976766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6499377, nsv6509115, nsv6506509
Samples
Known GenesCLEC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2943n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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