A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21334



Internal ID15828551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19298272..19298369hg38UCSC Ensembl
Outerchr14:19297693..19298780hg38UCSC Ensembl
Innerchr14:19885951..19886048hg19UCSC Ensembl
Outerchr14:19885372..19886465hg19UCSC Ensembl
Innerchr14:18955951..18956048hg18UCSC Ensembl
Outerchr14:18955372..18956465hg18UCSC Ensembl
Innerchr14:18955951..18956048hg17UCSC Ensembl
Outerchr14:18955372..18956465hg17UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381088
hg191094
hg181094
hg171094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA10839
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)nssv21334
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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