A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941103



Internal ID21361172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44047485..44047884hg38UCSC Ensembl
chr20:42676125..42676524hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179370
SamplesHG002
Known GenesTOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941103
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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