A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092578



Internal ID21280074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:112710591..112714804hg38UCSC Ensembl
Innerchr12:113148396..113152609hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg384214
hg194214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110538
Supporting Variants
Samplessample292
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092578
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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