A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926424



Internal ID21346494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63340338..63340533hg38UCSC Ensembl
chr20:61971690..61971885hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177959
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926424
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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