A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093109



Internal ID21281450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16893707..16904889hg38UCSC Ensembl
Innerchr11:16915254..16926436hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811183
hg1911183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112580
Supporting Variants
Samplessample312
Known GenesPLEKHA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093109
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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