A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21476



Internal ID15841144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21974192..22005780hg38UCSC Ensembl
Innerchr15:22262143..22293731hg19UCSC Ensembl
Innerchr15:19763507..19795095hg18UCSC Ensembl
Innerchr15:19763507..19795095hg17UCSC Ensembl
Outerchr15:19663241..19795441hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3831589
hg1931589
hg1831589
hg17132201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19007
Known GenesLOC727924
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)nssv21476
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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