A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27566



Internal ID15487369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44666761..44667127hg38UCSC Ensembl
Outerchr19:44666139..44670726hg38UCSC Ensembl
Innerchr19:45170030..45170396hg19UCSC Ensembl
Outerchr19:45169407..45173998hg19UCSC Ensembl
Innerchr19:49861870..49862236hg18UCSC Ensembl
Outerchr19:49861247..49865838hg18UCSC Ensembl
Innerchr19:49861870..49862236hg17UCSC Ensembl
Outerchr19:49861247..49865838hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg384588
hg194592
hg184592
hg174592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9736
Supporting Variants
SamplesNA18517
Known GenesPVR
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)nssv27566
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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