A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23761



Internal ID15843905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47010436..47070027hg38UCSC Ensembl
Outerchr10:47009885..47071817hg38UCSC Ensembl
Innerchr10:48669335..48728926hg19UCSC Ensembl
Outerchr10:48667545..48729477hg19UCSC Ensembl
Innerchr10:48289341..48348932hg18UCSC Ensembl
Outerchr10:48287551..48349483hg18UCSC Ensembl
Innerchr10:48289341..48348932hg17UCSC Ensembl
Outerchr10:48287551..48349483hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3861933
hg1961933
hg1861933
hg1761933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19221
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)nssv23761
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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