A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19060



Internal ID15831877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20074311..20097807hg38UCSC Ensembl
Outerchr15:20073972..20107136hg38UCSC Ensembl
Innerchr15:20279564..20303060hg19UCSC Ensembl
Outerchr15:20279225..20312389hg19UCSC Ensembl
Innerchr15:18539578..18563074hg18UCSC Ensembl
Outerchr15:18539239..18572403hg18UCSC Ensembl
Innerchr15:18539578..18563074hg17UCSC Ensembl
Outerchr15:18539239..18572403hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3833165
hg1933165
hg1833165
hg1733165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12802
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)nssv19060
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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