A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091132



Internal ID21290668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131909126..131910965hg38UCSC Ensembl
Innerchr11:131779020..131780859hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113083
Supporting Variants
Samplessample62
Known GenesNTM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091132
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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