A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10260



Internal ID15845223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:36014997..36016553hg38UCSC Ensembl
Outerchr3:36056489..36058045hg19UCSC Ensembl
Outerchr3:36031493..36033049hg18UCSC Ensembl
Outerchr3:36031493..36033049hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381557
hg191557
hg181557
hg171557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28769
SamplesNA07029
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)nsv10260
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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