A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19859



Internal ID15496556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133630853..133653672hg38UCSC Ensembl
Outerchr10:133629008..133655743hg38UCSC Ensembl
Innerchr10:135444357..135467176hg19UCSC Ensembl
Outerchr10:135442512..135469247hg19UCSC Ensembl
Innerchr10:135294347..135317166hg18UCSC Ensembl
Outerchr10:135292502..135319237hg18UCSC Ensembl
Innerchr10:135333238..135356057hg17UCSC Ensembl
Outerchr10:135331393..135358128hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3826736
hg1926736
hg1826736
hg1726736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8752
Supporting Variants
SamplesNA19173
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)nssv19859
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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