A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090701



Internal ID21272900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:174824473..175203194hg38UCSC Ensembl
Innerchr4:175745624..176124345hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38378722
hg19378722
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110448
Supporting Variants
Samplessample184
Known GenesADAM29, GLRA3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090701
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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