A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117193



Internal ID21300459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157389092..157394694hg38UCSC Ensembl
Innerchr7:157181786..157187388hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385603
hg195603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083448
Samplessample108
Known GenesDNAJB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117193
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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