A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110314



Internal ID21293580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15469209..15473359hg38UCSC Ensembl
Innerchr6:15469440..15473590hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384151
hg194151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1013n145
Supporting Variantsnssv14083816, nssv14083956
Samplessample417, sample385
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110314
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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