A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898811



Internal ID6305822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:12657513..12924960hg19UCSC Ensembl
Outerchr12:12655443..12928295hg19UCSC Ensembl
Innerchr12:12548780..12816227hg18UCSC Ensembl
Outerchr12:12546710..12819562hg18UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1549584
SamplesMS18274
Known GenesAPOLD1, CDKN1B, CREBL2, DUSP16, GPR19, MIR613
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898811
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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