A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931189



Internal ID21351258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50452075..50452136hg38UCSC Ensembl
chr20:49068612..49068673hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179579
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931189
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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