A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117890



Internal ID21301156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14435529..14442268hg38UCSC Ensembl
Innerchr11:14457075..14463814hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386740
hg196740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv192n145
Supporting Variantsnssv14090211, nssv14090266
Samplessample400, sample383
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117890
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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