A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990182



Internal ID21899525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85451375..85451442hg38UCSC Ensembl
chr2:85678498..85678565hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990182
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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