A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22191



Internal ID15838236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47476723..47476933hg38UCSC Ensembl
Outerchr10:47476235..47477050hg38UCSC Ensembl
Innerchr10:48262429..48262639hg19UCSC Ensembl
Outerchr10:48262312..48263127hg19UCSC Ensembl
Innerchr10:47882435..47882645hg18UCSC Ensembl
Outerchr10:47882318..47883133hg18UCSC Ensembl
Innerchr10:47882435..47882645hg17UCSC Ensembl
Outerchr10:47882318..47883133hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38816
hg19816
hg18816
hg17816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18860
Known GenesANXA8
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)nssv22191
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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