A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112681



Internal ID21295947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66125246..66128201hg38UCSC Ensembl
Innerchr7:65590233..65593188hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382956
hg192956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108n145
Supporting Variantsnssv14083379, nssv14086658, nssv14085084, nssv14084157, nssv14083408, nssv14085384, nssv14086751
Samplessample322, sample123, sample95, sample178, sample345, sample243, sample99
Known GenesCRCP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112681
Frequency
Sample Size467
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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