A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21987



Internal ID15841822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73674431..73697118hg38UCSC Ensembl
Outerchr10:73672835..73697852hg38UCSC Ensembl
Innerchr10:75434189..75456876hg19UCSC Ensembl
Outerchr10:75432593..75457610hg19UCSC Ensembl
Innerchr10:75104195..75126882hg18UCSC Ensembl
Outerchr10:75102599..75127616hg18UCSC Ensembl
Innerchr10:75104195..75126882hg17UCSC Ensembl
Outerchr10:75102599..75127616hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3825018
hg1925018
hg1825018
hg1725018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8688
Supporting Variants
SamplesNA19132
Known GenesAGAP5
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)nssv21987
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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