A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898922



Internal ID6305933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25282504..25401822hg19UCSC Ensembl
Outerchr12:25274593..25408047hg19UCSC Ensembl
Innerchr12:25173771..25293089hg18UCSC Ensembl
Outerchr12:25165860..25299314hg18UCSC 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 Variantsnssv1591751, nssv1579859
SamplesIS35181, IS39011
Known GenesCASC1, KRAS, LYRM5
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898922
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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