A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882863



Internal ID22657840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109224828..109227632hg38UCSC Ensembl
chr1:109767450..109770254hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382805
hg192805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369502
Samples
Known GenesSARS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882863
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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