A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9736



Internal ID15500962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:44666139..44670726hg38UCSC Ensembl
Outerchr19:45169407..45173998hg19UCSC Ensembl
Outerchr19:49861247..49865838hg18UCSC 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 StatusM
Merged Variants
Supporting Variantsnssv27566
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)nsv9736
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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