A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107582



Internal ID21292001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48482589..48495288hg38UCSC Ensembl
Innerchr4:48484606..48497305hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110529
Supporting Variants
Samplessample81
Known GenesSLC10A4, ZAR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107582
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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