A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116089



Internal ID21299355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9873420..9878563hg38UCSC Ensembl
Innerchr6:9873653..9878796hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg385144
hg195144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083978
Samplessample421
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116089
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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