A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24405



Internal ID15496875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79715252..79741233hg38UCSC Ensembl
Outerchr10:79714514..79741624hg38UCSC Ensembl
Innerchr10:81475008..81500989hg19UCSC Ensembl
Outerchr10:81474270..81501380hg19UCSC Ensembl
Innerchr10:81145014..81170995hg18UCSC Ensembl
Outerchr10:81144276..81171386hg18UCSC Ensembl
Innerchr10:81145014..81170995hg17UCSC Ensembl
Outerchr10:81144276..81171386hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3827111
hg1927111
hg1827111
hg1727111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8697
Supporting Variants
SamplesNA19221
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)nssv24405
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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