A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114367



Internal ID21297633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158212796..158231364hg38UCSC Ensembl
Innerchr6:158633828..158652396hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3818569
hg1918569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086404
Samplessample138
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114367
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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