A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803039



Internal ID21248377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62291827..62291827hg38UCSC Ensembl
chr20:60866883..60866883hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707492
Samples
Known GenesOSBPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803039
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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