A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8721



Internal ID15846633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:87469689..87500750hg38UCSC Ensembl
Outerchr10:89229446..89260507hg19UCSC Ensembl
Outerchr10:89219426..89250487hg18UCSC Ensembl
Outerchr10:89219426..89250487hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3831062
hg1931062
hg1831062
hg1731062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17779, nssv19555, nssv19216, nssv18714, nssv19525, nssv24561
SamplesNA18980, NA18975, NA18572, NA19221, 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)nsv8721
Frequency
Sample Size31
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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