A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11983



Internal ID15833532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24788244..24789267hg38UCSC Ensembl
Outerchr3:24787755..24791067hg38UCSC Ensembl
Innerchr3:24829735..24830758hg19UCSC Ensembl
Outerchr3:24829246..24832558hg19UCSC Ensembl
Innerchr3:24804739..24805762hg18UCSC Ensembl
Outerchr3:24804250..24807562hg18UCSC Ensembl
Innerchr3:24804739..24805762hg17UCSC Ensembl
Outerchr3:24804250..24807562hg17UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg383313
hg193313
hg183313
hg173313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10255
Supporting Variants
SamplesNA18504
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)nssv11983
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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