A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089225



Internal ID21279798
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 StatusS
Merged Variantsnsv3113972
Supporting Variants
Samplessample289
Known GenesRCAN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089225
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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