A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7982



Internal ID15499208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158234675..158238091hg38UCSC Ensembl
Outerchr6:158655707..158659123hg19UCSC Ensembl
Outerchr6:158575695..158579111hg18UCSC Ensembl
Outerchr6:158626116..158629532hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383417
hg193417
hg183417
hg173417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15239
SamplesNA19173
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)nsv7982
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer