A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026



Internal ID15494819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45873512..45914174hg38UCSC Ensembl
Outerchr10:45873244..45915677hg38UCSC Ensembl
Innerchr10:46368960..46409622hg19UCSC Ensembl
Outerchr10:46368692..46411125hg19UCSC Ensembl
Innerchr10:45688966..45729628hg18UCSC Ensembl
Outerchr10:45688698..45731131hg18UCSC Ensembl
Innerchr10:45688966..45729628hg17UCSC Ensembl
Outerchr10:45688698..45731131hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3842434
hg1942434
hg1842434
hg1742434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8631
Supporting Variants
SamplesNA19007
Known Genes
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)nssv18026
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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