A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110827



Internal ID21294093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143835616..143839122hg38UCSC Ensembl
Innerchr2:144593185..144596691hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383507
hg193507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv651n145
Supporting Variantsnssv14103761
Samplessample102
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110827
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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