A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111914



Internal ID21295180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17803032..17806058hg38UCSC Ensembl
Innerchr7:17842655..17845681hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg383027
hg193027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1099n145
Supporting Variantsnssv14085017
Samplessample404
Known GenesSNX13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111914
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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