A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11832



Internal ID15486140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37860745..37862719hg38UCSC Ensembl
Outerchr3:37860290..37863364hg38UCSC Ensembl
Innerchr3:37902236..37904210hg19UCSC Ensembl
Outerchr3:37901781..37904855hg19UCSC Ensembl
Innerchr3:37877240..37879214hg18UCSC Ensembl
Outerchr3:37876785..37879859hg18UCSC Ensembl
Innerchr3:37877240..37879214hg17UCSC Ensembl
Outerchr3:37876785..37879859hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg383075
hg193075
hg183075
hg173075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10262
Supporting Variants
SamplesNA18502
Known GenesCTDSPL
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)nssv11832
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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