A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092016



Internal ID21273724
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 StatusS
Merged Variantsnsv3115964
Supporting Variants
Samplessample196
Known GenesSLC10A4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092016
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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