A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985206



Internal ID21894549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86807346..86807543hg38UCSC Ensembl
chr1:87273029..87273226hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985206
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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