A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088091



Internal ID21282515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20794562..20804552hg38UCSC Ensembl
Innerchr9:20794561..20804551hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389991
hg199991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113893
Supporting Variants
Samplessample328
Known GenesFOCAD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088091
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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