A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113972



Internal ID21297238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:46489526..46492983hg38UCSC Ensembl
Innerchr6:46457263..46460720hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg383458
hg193458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089225
Samplessample289
Known GenesRCAN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113972
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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