A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1394n71



Internal ID6319014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25357680..25408047hg19UCSC Ensembl
chr12:25248947..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 Variantsnsv898925, nsv898926, nsv898923, nsv898924
SamplesIS30969, IS30532, IS31205, SP54030, IS31563, IS37393, MS18847, IS40067, IS38183
Known GenesKRAS, LYRM5
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1394n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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