A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25530



Internal ID15839664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101919204..101945117hg38UCSC Ensembl
Outerchr15:101911464..101948646hg38UCSC Ensembl
Innerchr15:102459407..102485320hg19UCSC Ensembl
Outerchr15:102451667..102488849hg19UCSC Ensembl
Innerchr15:100276930..100302843hg18UCSC Ensembl
Outerchr15:100269190..100306372hg18UCSC Ensembl
Innerchr15:100276930..100302843hg17UCSC Ensembl
Outerchr15:100269190..100306372hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3837183
hg1937183
hg1837183
hg1737183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9315
Supporting Variants
SamplesNA18972
Known GenesOR4F4
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)nssv25530
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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