A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22616



Internal ID15841502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91376599..91377297hg38UCSC Ensembl
Outerchr15:91375395..91377981hg38UCSC Ensembl
Innerchr15:91919829..91920527hg19UCSC Ensembl
Outerchr15:91918625..91921211hg19UCSC Ensembl
Innerchr15:89720833..89721531hg18UCSC Ensembl
Outerchr15:89719629..89722215hg18UCSC Ensembl
Innerchr15:89720833..89721531hg17UCSC Ensembl
Outerchr15:89719629..89722215hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382587
hg192587
hg182587
hg172587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9297
Supporting Variants
SamplesNA19007
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)nssv22616
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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