A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089960



Internal ID21280567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3926334..3949559hg38UCSC Ensembl
Innerchr11:3947564..3970789hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3823226
hg1923226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116515
Supporting Variants
Samplessample3
Known GenesSTIM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089960
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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