A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26810



Internal ID15497500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103886275..103895520hg38UCSC Ensembl
Outerchr14:103885835..103896606hg38UCSC Ensembl
Innerchr14:104352612..104361857hg19UCSC Ensembl
Outerchr14:104352172..104362943hg19UCSC Ensembl
Innerchr14:103422365..103431610hg18UCSC Ensembl
Outerchr14:103421925..103432696hg18UCSC Ensembl
Innerchr14:103422365..103431610hg17UCSC Ensembl
Outerchr14:103421925..103432696hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3810772
hg1910772
hg1810772
hg1710772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9174
Supporting Variants
SamplesNA19221
Known Genes
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)nssv26810
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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