A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23676



Internal ID15843886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48215863..48239037hg19UCSC Ensembl
Outerchr10:48215751..48239616hg19UCSC Ensembl
Innerchr10:47835869..47859043hg18UCSC Ensembl
Outerchr10:47835757..47859622hg18UCSC Ensembl
Innerchr10:47835869..47859043hg17UCSC Ensembl
Outerchr10:47835757..47859622hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1923866
hg1823866
hg1723866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19221
Known GenesAGAP9
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)nssv23676
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