A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107794



Internal ID21292777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47178283..47180271hg38UCSC Ensembl
Innerchr1:47643955..47645943hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115415
Supporting Variants
Samplessample91
Known GenesLINC00853
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107794
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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