A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117119



Internal ID21300385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144226013..144235117hg38UCSC Ensembl
Innerchr6:144547149..144556253hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg389105
hg199105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087732
Samplessample225
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117119
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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