A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25666



Internal ID15838111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22174724..22277176hg38UCSC Ensembl
Outerchr15:22174467..22277794hg38UCSC Ensembl
Innerchr15:22462675..22565127hg19UCSC Ensembl
Outerchr15:22462418..22565745hg19UCSC Ensembl
Innerchr15:19964039..20066491hg18UCSC Ensembl
Outerchr15:19963782..20067109hg18UCSC Ensembl
Innerchr15:19964039..20066491hg17UCSC Ensembl
Outerchr15:19963782..20067109hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38103328
hg19103328
hg18103328
hg17103328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18860
Known GenesREREP3
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)nssv25666
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