A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8603



Internal ID15846515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7051040..7098102hg38UCSC Ensembl
Outerchr10:7093002..7140064hg19UCSC Ensembl
Outerchr10:7133008..7180070hg18UCSC Ensembl
Outerchr10:7133008..7180070hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3847063
hg1947063
hg1847063
hg1747063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21584
SamplesNA18517
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)nsv8603
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