A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21385



Internal ID15840842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109710139..109710592hg38UCSC Ensembl
Outerchr13:109709163..109711111hg38UCSC Ensembl
Innerchr13:110362486..110362939hg19UCSC Ensembl
Outerchr13:110361510..110363458hg19UCSC Ensembl
Innerchr13:109160487..109160940hg18UCSC Ensembl
Outerchr13:109159511..109161459hg18UCSC Ensembl
Innerchr13:109160487..109160940hg17UCSC Ensembl
Outerchr13:109159511..109161459hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381949
hg191949
hg181949
hg171949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9107
Supporting Variants
SamplesNA18980
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)nssv21385
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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