A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3228n223



Internal ID22806196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65126001..65133166hg38UCSC Ensembl
chr17:63122119..63129284hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg387166
hg197166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6515759, nsv6531155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3228n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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