A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22337



Internal ID15489306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49479402..49487177hg38UCSC Ensembl
Outerchr15:49442238..49517268hg38UCSC Ensembl
Innerchr15:49771599..49779374hg19UCSC Ensembl
Outerchr15:49734435..49809465hg19UCSC Ensembl
Innerchr15:47558891..47566666hg18UCSC Ensembl
Outerchr15:47521727..47596757hg18UCSC Ensembl
Innerchr15:47558891..47566666hg17UCSC Ensembl
Outerchr15:47521727..47596757hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3875031
hg1975031
hg1875031
hg1775031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9263
Supporting Variants
SamplesNA18563
Known GenesFAM227B, FGF7
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)nssv22337
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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