A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21797



Internal ID15836139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19730805..19907202hg38UCSC Ensembl
Outerchr14:19723662..19907877hg38UCSC Ensembl
Innerchr14:20198964..20375361hg19UCSC Ensembl
Outerchr14:20191821..20376036hg19UCSC Ensembl
Innerchr14:19268804..19445201hg18UCSC Ensembl
Outerchr14:19261661..19445876hg18UCSC Ensembl
Innerchr14:19268804..19445201hg17UCSC Ensembl
Outerchr14:19261661..19445876hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38184216
hg19184216
hg18184216
hg17184216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA18563
Known GenesOR4K2, OR4M1, 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)nssv21797
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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