A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17975



Internal ID15828948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2862850..2865159hg38UCSC Ensembl
Outerchr11:2862153..2866253hg38UCSC Ensembl
Innerchr11:2884080..2886389hg19UCSC Ensembl
Outerchr11:2883383..2887483hg19UCSC Ensembl
Innerchr11:2840656..2842965hg18UCSC Ensembl
Outerchr11:2839959..2844059hg18UCSC Ensembl
Innerchr11:2840656..2842965hg17UCSC Ensembl
Outerchr11:2839959..2844059hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384101
hg194101
hg184101
hg174101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8765
Supporting Variants
SamplesNA10847
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)nssv17975
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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