A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112888



Internal ID21296154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145219396..145224032hg38UCSC Ensembl
Innerchr7:144916489..144921125hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384637
hg194637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1139n145
Supporting Variantsnssv14083247
Samplessample69
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112888
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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