A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986214



Internal ID21895557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139090668..139090722hg38UCSC Ensembl
chr2:139848238..139848292hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986214
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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