A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24520



Internal ID15834121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19730805..19783110hg38UCSC Ensembl
Outerchr14:19723662..19783868hg38UCSC Ensembl
Innerchr14:20198964..20251269hg19UCSC Ensembl
Outerchr14:20191821..20252027hg19UCSC Ensembl
Innerchr14:19268804..19321109hg18UCSC Ensembl
Outerchr14:19261661..19321867hg18UCSC Ensembl
Innerchr14:19268804..19321109hg17UCSC Ensembl
Outerchr14:19261661..19321867hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3860207
hg1960207
hg1860207
hg1760207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9117
Supporting Variants
SamplesNA18517
Known GenesOR4M1, 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)nssv24520
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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