A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867828



Internal ID22642763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16852781..16863362hg38UCSC Ensembl
chr2:17034048..17044629hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3810582
hg1910582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867828
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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