A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108773



Internal ID21270973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27854131..27861688hg38UCSC Ensembl
Innerchr5:27854238..27861795hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg387558
hg197558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111898
Supporting Variants
Samplessample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108773
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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