A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898886



Internal ID6305897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21355537..21449068hg19UCSC Ensembl
Outerchr12:21354494..21450250hg19UCSC Ensembl
Innerchr12:21246804..21340335hg18UCSC Ensembl
Outerchr12:21245761..21341517hg18UCSC 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 Variantsnssv1556642
SamplesMS22104
Known GenesSLCO1A2, SLCO1B1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898886
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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