A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21702



Internal ID15486444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100738803..100742606hg38UCSC Ensembl
Outerchr10:100738036..100743045hg38UCSC Ensembl
Innerchr10:102498560..102502363hg19UCSC Ensembl
Outerchr10:102497793..102502802hg19UCSC Ensembl
Innerchr10:102488550..102492353hg18UCSC Ensembl
Outerchr10:102487783..102492792hg18UCSC Ensembl
Innerchr10:102488550..102492353hg17UCSC Ensembl
Outerchr10:102487783..102492792hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg385010
hg195010
hg185010
hg175010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8725
Supporting Variants
SamplesNA18502
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)nssv21702
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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