A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898883



Internal ID6305894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21295612..21450445hg19UCSC Ensembl
Outerchr12:21294293..21450917hg19UCSC Ensembl
Innerchr12:21186879..21341712hg18UCSC Ensembl
Outerchr12:21185560..21342184hg18UCSC 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 Variantsnssv1519657
SamplesSP50101
Known GenesSLCO1A2, SLCO1B1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898883
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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