A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094835



Internal ID21285876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9956791..10101435hg38UCSC Ensembl
Innerchr4:9958415..10103059hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38144645
hg19144645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113157
Supporting Variants
Samplessample380
Known GenesMIR3138, SLC2A9, WDR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094835
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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