A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26929



Internal ID15487036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39893026..39894515hg38UCSC Ensembl
Outerchr19:39892005..39894901hg38UCSC Ensembl
Innerchr19:40399354..40400843hg19UCSC Ensembl
Outerchr19:40398329..40401229hg19UCSC Ensembl
Innerchr19:45091194..45092683hg18UCSC Ensembl
Outerchr19:45090169..45093069hg18UCSC Ensembl
Innerchr19:45091194..45092683hg17UCSC Ensembl
Outerchr19:45090169..45093069hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382897
hg192901
hg182901
hg172901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9725
Supporting Variants
SamplesNA18504
Known GenesFCGBP
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)nssv26929
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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