A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572



Internal ID15838718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48880401..48909209hg19UCSC Ensembl
Outerchr10:48879345..48910778hg19UCSC Ensembl
Innerchr10:48500407..48529215hg18UCSC Ensembl
Outerchr10:48499351..48530784hg18UCSC Ensembl
Innerchr10:48500407..48529215hg17UCSC Ensembl
Outerchr10:48499351..48530784hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1931434
hg1831434
hg1731434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18942
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)nssv17572
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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