A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898884



Internal ID6305895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21310009..21316213hg19UCSC Ensembl
Outerchr12:21309714..21317352hg19UCSC Ensembl
Innerchr12:21201276..21207480hg18UCSC Ensembl
Outerchr12:21200981..21208619hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1508072, nssv1515146
SamplesSP56126, SP54579
Known GenesSLCO1B1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898884
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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