A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10825



Internal ID15845788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32057955..32061815hg38UCSC Ensembl
Outerchr6:32025732..32029592hg19UCSC Ensembl
Outerchr6:32133710..32137570hg18UCSC Ensembl
Outerchr6:32133710..32137570hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383861
hg193861
hg183861
hg173861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14518
SamplesNA19144
Known GenesTNXB
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)nsv10825
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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