A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv899121



Internal ID6306132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:58087486..58166403hg19UCSC Ensembl
Outerchr12:58079825..58177292hg19UCSC Ensembl
Innerchr12:56373753..56452670hg18UCSC Ensembl
Outerchr12:56366092..56463559hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1585954
SamplesIS37646
Known GenesAGAP2, CDK4, CYP27B1, LOC100130776, MARCH9, METTL1, METTL21B, OS9, TSFM, TSPAN31
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv899121
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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