A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19366



Internal ID15488689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133477389..133480935hg38UCSC Ensembl
Outerchr10:133476534..133481352hg38UCSC Ensembl
Innerchr10:135290893..135294439hg19UCSC Ensembl
Outerchr10:135290038..135294856hg19UCSC Ensembl
Innerchr10:135140883..135144429hg18UCSC Ensembl
Outerchr10:135140028..135144846hg18UCSC Ensembl
Innerchr10:135179774..135183320hg17UCSC Ensembl
Outerchr10:135178919..135183737hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg384819
hg194819
hg184819
hg174819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8752
Supporting Variants
SamplesNA18552
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)nssv19366
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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