A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26654



Internal ID15843489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19730805..19863095hg38UCSC Ensembl
Outerchr14:19723662..19863720hg38UCSC Ensembl
Innerchr14:20198964..20331254hg19UCSC Ensembl
Outerchr14:20191821..20331879hg19UCSC Ensembl
Innerchr14:19268804..19401094hg18UCSC Ensembl
Outerchr14:19261661..19401719hg18UCSC Ensembl
Innerchr14:19268804..19401094hg17UCSC Ensembl
Outerchr14:19261661..19401719hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38140059
hg19140059
hg18140059
hg17140059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA19221
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)nssv26654
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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