A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094652



Internal ID21283678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26858768..26862914hg38UCSC Ensembl
Innerchr4:26860390..26864536hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384147
hg194147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111041
Supporting Variants
Samplessample348
Known GenesSTIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094652
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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