A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092936



Internal ID21280313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89630429..89634900hg38UCSC Ensembl
Innerchr1:90095988..90100459hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg384472
hg194472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115440
Supporting Variants
Samplessample296
Known GenesFLJ27354, LRRC8C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092936
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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