A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9656



Internal ID15500882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:303742..313997hg38UCSC Ensembl
Outerchr19:303742..313997hg19UCSC Ensembl
Outerchr19:254742..264997hg18UCSC Ensembl
Outerchr19:254742..264997hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810256
hg1910256
hg1810256
hg1710256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26418
SamplesNA12155
Known GenesMIER2
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)nsv9656
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer