A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093862



Internal ID21286269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:55365707..55377086hg38UCSC Ensembl
Innerchr12:55759491..55770870hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3811380
hg1911380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113716
Supporting Variants
Samplessample386
Known GenesOR6C75
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093862
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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