A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18590



Internal ID15837421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50191539..50192737hg38UCSC Ensembl
Outerchr10:50191128..50193057hg38UCSC Ensembl
Innerchr10:48006008..48007218hg19UCSC Ensembl
Outerchr10:48005597..48007527hg19UCSC Ensembl
Innerchr10:47526014..47527224hg18UCSC Ensembl
Outerchr10:47525603..47527533hg18UCSC Ensembl
Innerchr10:47526014..47527224hg17UCSC Ensembl
Outerchr10:47525603..47527533hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381930
hg191931
hg181931
hg171931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18853
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)nssv18590
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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