A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901686



Internal ID22676838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163504158..163514584hg38UCSC Ensembl
chr2:164360668..164371094hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3810427
hg1910427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901686
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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