A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932188



Internal ID22707482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10321544..10322423hg38UCSC Ensembl
chr20:10302192..10303071hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932188
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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