A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117006



Internal ID21300272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99842998..99847089hg38UCSC Ensembl
Innerchr7:99440621..99444712hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384092
hg194092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083212
Samplessample61
Known GenesCYP3A43
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117006
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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