A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv870819



Internal ID6277830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12234622..12265575hg19UCSC Ensembl
Outerchr1:12233754..12267265hg19UCSC Ensembl
Innerchr1:12157209..12188162hg18UCSC Ensembl
Outerchr1:12156341..12189852hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1506983, nssv1506952
SamplesSP54442, SP54448
Known GenesMIR4632, TNFRSF1B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv870819
Frequency
Sample Size6533
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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