A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19841



Internal ID15832226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20753972..20761873hg38UCSC Ensembl
Outerchr15:20753120..20762210hg38UCSC Ensembl
Innerchr15:20959301..20967202hg19UCSC Ensembl
Outerchr15:20958449..20967539hg19UCSC Ensembl
Innerchr15:19219313..19227233hg18UCSC Ensembl
Outerchr15:19218462..19227570hg18UCSC Ensembl
Innerchr15:19219313..19227233hg17UCSC Ensembl
Outerchr15:19218462..19227570hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg389091
hg199091
hg189109
hg179109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12872
Known GenesNBEAP1
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)nssv19841
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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