A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19508



Internal ID15484229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3068025..3069249hg38UCSC Ensembl
Outerchr10:3066770..3070337hg38UCSC Ensembl
Innerchr10:3110217..3111441hg19UCSC Ensembl
Outerchr10:3108962..3112529hg19UCSC Ensembl
Innerchr10:3100217..3101441hg18UCSC Ensembl
Outerchr10:3098962..3102529hg18UCSC Ensembl
Innerchr10:3100217..3101441hg17UCSC Ensembl
Outerchr10:3098962..3102529hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg383568
hg193568
hg183568
hg173568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8595
Supporting Variants
SamplesNA12155
Known GenesPFKP
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)nssv19508
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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