A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114731



Internal ID21297997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47082237..47152018hg38UCSC Ensembl
Innerchr1:47547909..47617690hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3869782
hg1969782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082950
Samplessample172
Known GenesCYP4A22, CYP4Z1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114731
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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