A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089343



Internal ID21267832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143782018..143966866hg38UCSC Ensembl
Innerchr4:144703171..144888019hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38184849
hg19184849
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112507
Supporting Variants
Samplessample117
Known GenesGYPE
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089343
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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