A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7n171



Internal ID22814369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19273804..19274256hg38UCSC Ensembl
chr20:19254448..19254900hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4392497, nsv4392498
Samples
Known GenesLOC100130264, SLC24A3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)dgv7n171
Frequency
Sample Size174
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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