A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206



Internal ID15841485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47186205..47255048hg19UCSC Ensembl
Outerchr10:47186041..47255093hg19UCSC Ensembl
Innerchr10:46606211..46675054hg18UCSC Ensembl
Outerchr10:46606047..46675099hg18UCSC Ensembl
Innerchr10:46606211..46675054hg17UCSC Ensembl
Outerchr10:46606047..46675099hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1969053
hg1869053
hg1769053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19007
Known GenesAGAP9, BMS1P2, BMS1P6
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv18206
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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