A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25140



Internal ID15832673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20636190..20643849hg38UCSC Ensembl
Outerchr15:20628545..20645618hg38UCSC Ensembl
Innerchr15:20841494..20849151hg19UCSC Ensembl
Outerchr15:20833848..20850920hg19UCSC Ensembl
Innerchr15:19101508..19109165hg18UCSC Ensembl
Outerchr15:19093862..19110934hg18UCSC Ensembl
Innerchr15:19101508..19109165hg17UCSC Ensembl
Outerchr15:19093862..19110934hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3817074
hg1917073
hg1817073
hg1717073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18502
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)nssv25140
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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