A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22073



Internal ID15839538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46707014..46779788hg38UCSC Ensembl
Innerchr10:48105976..48178715hg19UCSC Ensembl
Innerchr10:47725982..47798721hg18UCSC Ensembl
Innerchr10:47725982..47798721hg17UCSC Ensembl
Outerchr10:47574688..47799221hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3872775
hg1972740
hg1872740
hg17224534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18972
Known GenesCTSLP2
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)nssv22073
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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