A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21715



Internal ID15494088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73568178..73574863hg38UCSC Ensembl
Outerchr14:73564692..73575600hg38UCSC Ensembl
Innerchr14:74034882..74041567hg19UCSC Ensembl
Outerchr14:74031396..74042304hg19UCSC Ensembl
Innerchr14:73104635..73111320hg18UCSC Ensembl
Outerchr14:73101149..73112057hg18UCSC Ensembl
Innerchr14:73104635..73111320hg17UCSC Ensembl
Outerchr14:73101149..73112057hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810909
hg1910909
hg1810909
hg1710909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9153
Supporting Variants
SamplesNA18980
Known GenesACOT2
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)nssv21715
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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