A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898874



Internal ID6305885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21010048..21015760hg19UCSC Ensembl
Outerchr12:21008004..21016568hg19UCSC Ensembl
Innerchr12:20901315..20907027hg18UCSC Ensembl
Outerchr12:20899271..20907835hg18UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1562827, nssv1578893, nssv1551801, nssv1583796, nssv1567034, nssv1568578, nssv1568594, nssv1551351, nssv1568966, nssv1567977, nssv1583070, nssv1554636
SamplesIS34962, IS36656, MS25751, IS36244, MS18978, IS31041, IS31179, IS31306, IS31307, MS18847, MS20872, IS31373
Known GenesSLCO1B3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898874
Frequency
Sample Size6533
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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