A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22163



Internal ID15839541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47414973..47420772hg38UCSC Ensembl
Outerchr10:47414394..47421513hg38UCSC Ensembl
Innerchr10:48318590..48324389hg19UCSC Ensembl
Outerchr10:48317849..48324968hg19UCSC Ensembl
Innerchr10:47938596..47944395hg18UCSC Ensembl
Outerchr10:47937855..47944974hg18UCSC Ensembl
Innerchr10:47938596..47944395hg17UCSC Ensembl
Outerchr10:47937855..47944974hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg387120
hg197120
hg187120
hg177120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18972
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)nssv22163
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