A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21466



Internal ID15835550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20579152..20624726hg38UCSC Ensembl
Outerchr15:20579075..20625069hg38UCSC Ensembl
Innerchr15:20784475..20830029hg19UCSC Ensembl
Outerchr15:20784398..20830372hg19UCSC Ensembl
Innerchr15:19044489..19090043hg18UCSC Ensembl
Outerchr15:19044412..19090386hg18UCSC Ensembl
Innerchr15:19044489..19090043hg17UCSC Ensembl
Outerchr15:19044412..19090386hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3845995
hg1945975
hg1845975
hg1745975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18552
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)nssv21466
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