A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18356



Internal ID15841469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50147614..50154225hg38UCSC Ensembl
Outerchr10:50146258..50158011hg38UCSC Ensembl
Innerchr10:47963530..47968685hg19UCSC Ensembl
Outerchr10:47962177..47972471hg19UCSC Ensembl
Innerchr10:47483536..47488691hg18UCSC Ensembl
Outerchr10:47482183..47492477hg18UCSC Ensembl
Innerchr10:47483536..47488691hg17UCSC Ensembl
Outerchr10:47482183..47492477hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3811754
hg1910295
hg1810295
hg1710295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA19007
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)nssv18356
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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