A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9826



Internal ID15847738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63606039..63611302hg38UCSC Ensembl
Outerchr20:62237392..62242655hg19UCSC Ensembl
Outerchr20:61707836..61713099hg18UCSC Ensembl
Outerchr20:61707836..61713099hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385264
hg195264
hg185264
hg175264
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25202, nssv27585, nssv25199, nssv24678, nssv25656, nssv22025, nssv27201, nssv26542, nssv27707, nssv25517, nssv26016, nssv26949, nssv26164
SamplesNA11830, NA18504, NA12155, NA10839, NA10847, NA10863, NA18853, NA19132, NA18517, NA19144, NA12740, NA19173, NA18552
Known GenesGMEB2
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)nsv9826
Frequency
Sample Size31
Observed Gain1
Observed Loss12
Observed Complex0
Frequencyn/a


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