A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105215



Internal ID21278772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:47172510..47178968hg38UCSC Ensembl
Innerchr2:47399649..47406107hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg386459
hg196459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115908
Supporting Variants
Samplessample273
Known GenesCALM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105215
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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