A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19781



Internal ID15832286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20091127..20091174hg38UCSC Ensembl
Outerchr15:20090276..20092802hg38UCSC Ensembl
Innerchr15:20296380..20296427hg19UCSC Ensembl
Outerchr15:20295529..20298055hg19UCSC Ensembl
Innerchr15:18556394..18556441hg18UCSC Ensembl
Outerchr15:18555543..18558069hg18UCSC Ensembl
Innerchr15:18556394..18556441hg17UCSC Ensembl
Outerchr15:18555543..18558069hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382527
hg192527
hg182527
hg172527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12872
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)nssv19781
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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