A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9095



Internal ID15847007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:85118827..85132204hg38UCSC Ensembl
Outerchr13:85692962..85706339hg19UCSC Ensembl
Outerchr13:84590963..84604340hg18UCSC Ensembl
Outerchr13:84590963..84604340hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3813378
hg1913378
hg1813378
hg1713378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24362
SamplesNA18502
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)nsv9095
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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