A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19871



Internal ID15832036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20992779..20996708hg38UCSC Ensembl
Outerchr15:20991898..20996806hg38UCSC Ensembl
Innerchr15:21198108..21202037hg19UCSC Ensembl
Outerchr15:21197227..21202135hg19UCSC Ensembl
Innerchr15:19462767..19466696hg18UCSC Ensembl
Outerchr15:19461886..19466794hg18UCSC Ensembl
Innerchr15:19462767..19466696hg17UCSC Ensembl
Outerchr15:19461886..19466794hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384909
hg194909
hg184909
hg174909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12872
Known GenesCT60
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)nssv19871
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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