A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116099



Internal ID21299365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14435529..14443085hg38UCSC Ensembl
Innerchr11:14457075..14464631hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg387557
hg197557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv192n145
Supporting Variantsnssv14091783
Samplessample180
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116099
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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