A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933012



Internal ID21353081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57598460..57598510hg38UCSC Ensembl
chr20:56173516..56173566hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179395
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933012
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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