A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20209



Internal ID15837071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101864466..101906484hg38UCSC Ensembl
Outerchr15:101859658..101911464hg38UCSC Ensembl
Innerchr15:102404669..102446687hg19UCSC Ensembl
Outerchr15:102399861..102451667hg19UCSC Ensembl
Innerchr15:100222192..100264210hg18UCSC Ensembl
Outerchr15:100217384..100269190hg18UCSC Ensembl
Innerchr15:100222192..100264210hg17UCSC Ensembl
Outerchr15:100217384..100269190hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3851807
hg1951807
hg1851807
hg1751807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9315
Supporting Variants
SamplesNA18572
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)nssv20209
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