A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19285



Internal ID15840423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73666799..73697118hg38UCSC Ensembl
Outerchr10:73666766..73697852hg38UCSC Ensembl
Innerchr10:75426557..75456876hg19UCSC Ensembl
Outerchr10:75426524..75457610hg19UCSC Ensembl
Innerchr10:75096563..75126882hg18UCSC Ensembl
Outerchr10:75096530..75127616hg18UCSC Ensembl
Innerchr10:75096563..75126882hg17UCSC Ensembl
Outerchr10:75096530..75127616hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3831087
hg1931087
hg1831087
hg1731087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8688
Supporting Variants
SamplesNA18980
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)nssv19285
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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