A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23514



Internal ID15483167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32539000..32585606hg38UCSC Ensembl
Outerchr15:32538500..32585863hg38UCSC Ensembl
Innerchr15:32831201..32877807hg19UCSC Ensembl
Outerchr15:32830701..32878064hg19UCSC Ensembl
Innerchr15:30618493..30665099hg18UCSC Ensembl
Outerchr15:30617993..30665356hg18UCSC Ensembl
Innerchr15:30618493..30665099hg17UCSC Ensembl
Outerchr15:30617993..30665356hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3847364
hg1947364
hg1847364
hg1747364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9238
Supporting Variants
SamplesNA11830
Known GenesLOC100996255
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)nssv23514
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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