A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18710



Internal ID15837881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47145322..47147296hg38UCSC Ensembl
Outerchr10:47144132..47150836hg38UCSC Ensembl
Innerchr10:48592066..48594040hg19UCSC Ensembl
Outerchr10:48588526..48595230hg19UCSC Ensembl
Innerchr10:48212072..48214046hg18UCSC Ensembl
Outerchr10:48208532..48215236hg18UCSC Ensembl
Innerchr10:48212072..48214046hg17UCSC Ensembl
Outerchr10:48208532..48215236hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386705
hg196705
hg186705
hg176705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18853
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)nssv18710
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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