A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19654



Internal ID15482100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133641902..133646113hg38UCSC Ensembl
Outerchr10:133641495..133648240hg38UCSC Ensembl
Innerchr10:135455406..135459617hg19UCSC Ensembl
Outerchr10:135454999..135461744hg19UCSC Ensembl
Innerchr10:135305396..135309607hg18UCSC Ensembl
Outerchr10:135304989..135311734hg18UCSC Ensembl
Innerchr10:135344287..135348498hg17UCSC Ensembl
Outerchr10:135343880..135350625hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386746
hg196746
hg186746
hg176746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8752
Supporting Variants
SamplesNA10839
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)nssv19654
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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