A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010063



Internal ID18752594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46798533..46819446hg38UCSC Ensembl
Innerchr1:47264205..47285118hg19UCSC Ensembl
Innerchr1:47036792..47057705hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3820914
hg1920914
hg1820914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3473801, nssv3476936
Samples
Known GenesCYP4B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010063
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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