A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv883028



Internal ID6290039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149495253..149535255hg19UCSC Ensembl
Outerchr5:149492455..149544045hg19UCSC Ensembl
Innerchr5:149475446..149515448hg18UCSC Ensembl
Outerchr5:149472648..149524238hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1549676, nssv1537073
SamplesMS13095, MS18276
Known GenesCSF1R, PDGFRB
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv883028
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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