A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091231



Internal ID21272859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:22743868..22763861hg38UCSC Ensembl
Innerchr12:22896802..22916795hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3819994
hg1919994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115758
Supporting Variants
Samplessample183
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091231
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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