A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8237



Internal ID15846149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:153781012..154111761hg38UCSC Ensembl
Outerchr7:153478097..153808846hg19UCSC Ensembl
Outerchr7:153109030..153439779hg18UCSC Ensembl
Outerchr7:152915745..153246494hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38330750
hg19330750
hg18330750
hg17330750
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15622, nssv18402, nssv16255, nssv15744, nssv19484, nssv20070, nssv18643, nssv16285, nssv16986, nssv20040, nssv16653
SamplesNA18502, NA18980, NA18504, NA18942, NA07048, NA18975, NA10863, NA19221, NA18517
Known GenesDPP6
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)nsv8237
Frequency
Sample Size31
Observed Gain4
Observed Loss5
Observed Complex0
Frequencyn/a


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