A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv871961



Internal ID6278972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47881978..47907662hg19UCSC Ensembl
Outerchr1:47875627..47912628hg19UCSC Ensembl
Innerchr1:47654565..47680249hg18UCSC Ensembl
Outerchr1:47648214..47685215hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1509752
SamplesSP54956
Known GenesFOXD2, FOXE3, MGC12982
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv871961
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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