A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092531



Internal ID21279060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:96044963..96104419hg38UCSC Ensembl
Innerchr12:96438741..96498197hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3859457
hg1959457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115424
Supporting Variants
Samplessample277
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092531
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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