A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10808



Internal ID15499085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29680274..29685406hg38UCSC Ensembl
Outerchr6:29648051..29653183hg19UCSC Ensembl
Outerchr6:29756030..29761162hg18UCSC Ensembl
Outerchr6:29756030..29761162hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg385133
hg195133
hg185133
hg175133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15091
SamplesNA19240
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)nsv10808
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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