A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv886433



Internal ID6293444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99274066..99290592hg19UCSC Ensembl
Outerchr6:99270533..99292136hg19UCSC Ensembl
Innerchr6:99380787..99397313hg18UCSC Ensembl
Outerchr6:99377254..99398857hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510725
SamplesSP54988
Known GenesPOU3F2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv886433
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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