A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100770



Internal ID21285697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33270890..33312197hg38UCSC Ensembl
Innerchr20:31858696..31900003hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3841308
hg1941308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115344
Supporting Variants
Samplessample379
Known GenesBPIFB1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100770
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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