A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21805



Internal ID15840757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19994402..20002599hg38UCSC Ensembl
Outerchr15:19992945..20003612hg38UCSC Ensembl
Innerchr15:20199655..20207852hg19UCSC Ensembl
Outerchr15:20198198..20208865hg19UCSC Ensembl
Innerchr15:18459669..18467866hg18UCSC Ensembl
Outerchr15:18458212..18468879hg18UCSC Ensembl
Innerchr15:18459669..18467866hg17UCSC Ensembl
Outerchr15:18458212..18468879hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3810668
hg1910668
hg1810668
hg1710668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18980
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)nssv21805
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