A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21613



Internal ID15833279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93972..93972hg38UCSC Ensembl
Outerchr11:93219..94102hg38UCSC Ensembl
Innerchr11:93972..93972hg19UCSC Ensembl
Outerchr11:93219..94102hg19UCSC Ensembl
Innerchr11:83972..83972hg18UCSC Ensembl
Outerchr11:83219..84102hg18UCSC Ensembl
Innerchr11:83972..83972hg17UCSC Ensembl
Outerchr11:83219..84102hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38884
hg19884
hg18884
hg17884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8753
Supporting Variants
SamplesNA18504
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)nssv21613
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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