A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20182



Internal ID15839077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20626211..20998401hg38UCSC Ensembl
Outerchr15:20626192..20998839hg38UCSC Ensembl
Innerchr15:20831514..21203730hg19UCSC Ensembl
Outerchr15:20831495..21204168hg19UCSC Ensembl
Innerchr15:19091528..19468389hg18UCSC Ensembl
Outerchr15:19091509..19468827hg18UCSC Ensembl
Innerchr15:19091528..19468389hg17UCSC Ensembl
Outerchr15:19091509..19468827hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38372648
hg19372674
hg18377319
hg17377319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18942
Known GenesCT60, CXADRP2, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
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)nssv20182
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