A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115964



Internal ID21299230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48482589..48485073hg38UCSC Ensembl
Innerchr4:48484606..48487090hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg382485
hg192485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093425, nssv14092016
Samplessample196, sample289
Known GenesSLC10A4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115964
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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