A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091524



Internal ID21290376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:69238548..69241285hg38UCSC Ensembl
Innerchr12:69632328..69635065hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg382738
hg192738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110864
Supporting Variants
Samplessample59
Known GenesCPSF6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091524
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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