A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7935



Internal ID15845847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:81426794..81465251hg38UCSC Ensembl
Outerchr6:82136511..82174968hg19UCSC Ensembl
Outerchr6:82193230..82231687hg18UCSC Ensembl
Outerchr6:82193230..82231687hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3838458
hg1938458
hg1838458
hg1738458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033
SamplesNA18972
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)nsv7935
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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