A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898872



Internal ID6305883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21007718..21404832hg19UCSC Ensembl
Outerchr12:21000586..21413632hg19UCSC Ensembl
Innerchr12:20898985..21296099hg18UCSC Ensembl
Outerchr12:20891853..21304899hg18UCSC 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 Variantsnssv1576046, nssv1582670
SamplesIS36077, IS33864
Known GenesSLCO1B1, SLCO1B3, SLCO1B7
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898872
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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