A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113380



Internal ID21296646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:109063020..109065086hg38UCSC Ensembl
Innerchr6:109384223..109386289hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382067
hg192067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086332
Samplessample122
Known GenesSESN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113380
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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