A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8631



Internal ID15499857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45873244..45915677hg38UCSC Ensembl
Outerchr10:46368692..46411125hg19UCSC Ensembl
Outerchr10:45688698..45731131hg18UCSC Ensembl
Outerchr10:45688698..45731131hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3842434
hg1942434
hg1842434
hg1742434
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19277, nssv21651, nssv21621, nssv18026
SamplesNA18860, NA18563, NA19007
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)nsv8631
Frequency
Sample Size31
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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