A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20791



Internal ID15844701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47568360..47591872hg38UCSC Ensembl
Outerchr10:47567223..47592384hg38UCSC Ensembl
Innerchr10:47258351..47281882hg19UCSC Ensembl
Outerchr10:47257214..47282394hg19UCSC Ensembl
Innerchr10:46678357..46701888hg18UCSC Ensembl
Outerchr10:46677220..46702400hg18UCSC Ensembl
Innerchr10:46678357..46701888hg17UCSC Ensembl
Outerchr10:46677220..46702400hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3825162
hg1925181
hg1825181
hg1725181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19240
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)nssv20791
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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