A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9587



Internal ID15847499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:68079924..68170183hg38UCSC Ensembl
Outerchr17:66076031..66166324hg19UCSC Ensembl
Outerchr17:63587668..63677919hg18UCSC Ensembl
Outerchr17:63587668..63677919hg17UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3890260
hg1990294
hg1890252
hg1790252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24409
SamplesNA10839
Known GenesLINC00674
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)nsv9587
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