A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898880



Internal ID6305891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21291501..21318265hg19UCSC Ensembl
Outerchr12:21282953..21321482hg19UCSC Ensembl
Innerchr12:21182768..21209532hg18UCSC Ensembl
Outerchr12:21174220..21212749hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1541509
SamplesMS15341
Known GenesSLCO1B1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898880
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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