A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1860n223



Internal ID22804828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60242201..60245900hg38UCSC Ensembl
chr13:60816335..60820034hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6491047, nsv6476368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1860n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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