A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv910901



Internal ID6272828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5784867..5834377hg19UCSC Ensembl
Outerchr19:5781998..5836964hg19UCSC Ensembl
Innerchr19:5735867..5785377hg18UCSC Ensembl
Outerchr19:5732998..5787964hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510276
SamplesSP54956
Known GenesDUS3L, FUT6, NRTN, PRR22
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv910901
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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