A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114161



Internal ID21297427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:216033903..216039648hg38UCSC Ensembl
Innerchr2:216898626..216904371hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg385746
hg195746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101841
Samplessample17
Known GenesPECR
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114161
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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