A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090197



Internal ID21285757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5250295..5254229hg38UCSC Ensembl
Innerchr11:5271525..5275459hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383935
hg193935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117251
Supporting Variants
Samplessample379
Known GenesHBG2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090197
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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