A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8662



Internal ID15846574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:50656902..50701319hg38UCSC Ensembl
Outerchr10:52416662..52461079hg19UCSC Ensembl
Outerchr10:52086668..52131085hg18UCSC Ensembl
Outerchr10:52086668..52131085hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3844418
hg1944418
hg1844418
hg1744418
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18916, nssv24193
SamplesNA19221, NA18552
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)nsv8662
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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