A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117733



Internal ID21300999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57212554..57220475hg38UCSC Ensembl
Innerchr11:56980028..56987949hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387922
hg197922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091864
Samplessample213
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117733
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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