A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv883027



Internal ID6290038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149492296..149575855hg19UCSC Ensembl
Outerchr5:149489110..149577919hg19UCSC Ensembl
Innerchr5:149472489..149556048hg18UCSC Ensembl
Outerchr5:149469303..149558112hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1543447
SamplesMS16153
Known GenesCDX1, CSF1R, PDGFRB, SLC6A7
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv883027
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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