A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943642



Internal ID22719093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17185656..17185850hg38UCSC Ensembl
chr20:17166301..17166495hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943642
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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