A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520748



Internal ID21845107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41288757..41586263hg38UCSC Ensembl
chr2:41515897..41813403hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38297507
hg19297507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520748
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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