A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009338



Internal ID18751869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46892860..47089581hg38UCSC Ensembl
Innerchr1:47358532..47555253hg19UCSC Ensembl
Innerchr1:47131119..47327840hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38196722
hg19196722
hg18196722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3467495
Samples
Known GenesCYP4A11, CYP4X1, CYP4Z1, CYP4Z2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009338
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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