A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21938



Internal ID15830645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18595008..18911093hg38UCSC Ensembl
Outerchr14:18591020..18912561hg38UCSC Ensembl
Innerchr14:19371485..19496846hg19UCSC Ensembl
Outerchr14:19367497..19498314hg19UCSC Ensembl
Innerchr14:18441485..18566846hg18UCSC Ensembl
Outerchr14:18437497..18568314hg18UCSC Ensembl
Innerchr14:18441485..18566846hg17UCSC Ensembl
Outerchr14:18437497..18568314hg17UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38321542
hg19130818
hg18130818
hg17130818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA12155
Known GenesLOC642426, OR11H12
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)nssv21938
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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