A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5686n223



Internal ID22808654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18815497..18974957hg38UCSC Ensembl
chr5:18815606..18975066hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38159461
hg19159461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6393686, nsv6382877, nsv6382776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5686n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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