A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988163



Internal ID21897506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223726596..223726663hg38UCSC Ensembl
chr2:224591313..224591380hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988163
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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