A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118143



Internal ID21301409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143835872..143838414hg38UCSC Ensembl
Innerchr2:144593441..144595983hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg382543
hg192543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv651n145
Supporting Variantsnssv14103798
Samplessample112
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118143
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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