A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093699



Internal ID21282819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:102236664..102278877hg38UCSC Ensembl
Innerchr12:102630442..102672655hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3842214
hg1942214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118254
Supporting Variants
Samplessample332
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093699
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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