A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10726



Internal ID15845689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:99518205..99537200hg38UCSC Ensembl
Outerchr5:98853909..98872904hg19UCSC Ensembl
Outerchr5:98881808..98900803hg18UCSC Ensembl
Outerchr5:98881808..98900803hg17UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3818996
hg1918996
hg1818996
hg1718996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13936, nssv13986, nssv14528, nssv12790, nssv15983, nssv14619, nssv13525
SamplesNA18980, NA12155, NA12802, NA10863, NA12740, NA18972, NA18552
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)nsv10726
Frequency
Sample Size31
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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