A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8632



Internal ID15499858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45928396..45929593hg38UCSC Ensembl
Outerchr10:46423844..46425041hg19UCSC Ensembl
Outerchr10:45743850..45745047hg18UCSC Ensembl
Outerchr10:45743850..45745047hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381198
hg191198
hg181198
hg171198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056, nssv21681
SamplesNA18860, 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)nsv8632
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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