A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19113



Internal ID15827908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38686418..38695082hg38UCSC Ensembl
Outerchr10:38686187..38695536hg38UCSC Ensembl
Innerchr10:38979549..38988213hg19UCSC Ensembl
Outerchr10:38979318..38988667hg19UCSC Ensembl
Innerchr10:39019555..39028219hg18UCSC Ensembl
Outerchr10:39019324..39028673hg18UCSC Ensembl
Innerchr10:39019555..39028219hg17UCSC Ensembl
Outerchr10:39019324..39028673hg17UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg389350
hg199350
hg189350
hg179350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8620
Supporting Variants
SamplesNA07048
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)nssv19113
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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