A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8440



Internal ID15846352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33598658..33611084hg38UCSC Ensembl
Outerchr9:33598656..33611082hg19UCSC Ensembl
Outerchr9:33588656..33601082hg18UCSC Ensembl
Outerchr9:33588656..33601082hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3812427
hg1912427
hg1812427
hg1712427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15701
SamplesNA12872
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)nsv8440
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