A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117070



Internal ID21300336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16309399..16362465hg38UCSC Ensembl
Innerchr7:16349024..16402090hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3853067
hg1953067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1097n145
Supporting Variantsnssv14083342, nssv14086738, nssv14085627, nssv14084978
Samplessample396, sample343, sample302, sample89
Known GenesISPD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117070
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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