A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19702



Internal ID15839053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19716536..19829438hg38UCSC Ensembl
Outerchr14:19716201..19839319hg38UCSC Ensembl
Innerchr14:20184695..20297597hg19UCSC Ensembl
Outerchr14:20184360..20307478hg19UCSC Ensembl
Innerchr14:19254535..19367437hg18UCSC Ensembl
Outerchr14:19254200..19377318hg18UCSC Ensembl
Innerchr14:19254535..19367437hg17UCSC Ensembl
Outerchr14:19254200..19377318hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38123119
hg19123119
hg18123119
hg17123119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA18942
Known GenesOR4M1, OR4N2, OR4Q3
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)nssv19702
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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