A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111395



Internal ID21294661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10093414..10096601hg38UCSC Ensembl
Innerchr12:10246013..10249200hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg383188
hg193188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092744
Samplessample115
Known GenesCLEC1A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111395
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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