A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18714



Internal ID15839935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87473138..87499699hg38UCSC Ensembl
Outerchr10:87469689..87500750hg38UCSC Ensembl
Innerchr10:89232895..89259456hg19UCSC Ensembl
Outerchr10:89229446..89260507hg19UCSC Ensembl
Innerchr10:89222875..89249436hg18UCSC Ensembl
Outerchr10:89219426..89250487hg18UCSC Ensembl
Innerchr10:89222875..89249436hg17UCSC 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 StatusS
Merged Variantsnsv8721
Supporting Variants
SamplesNA18975
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)nssv18714
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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