A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113371



Internal ID21296637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143835616..143838846hg38UCSC Ensembl
Innerchr2:144593185..144596415hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383231
hg193231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv651n145
Supporting Variantsnssv14105667
Samplessample206
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113371
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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