A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1159884



Internal ID18955853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59006406..59043770hg38UCSC Ensembl
Outerchr11:59005164..59043992hg38UCSC Ensembl
Innerchr11:58773879..58811243hg19UCSC Ensembl
Outerchr11:58772637..58811465hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3838829
hg1938829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4030753
Samples
Known GenesLOC283194
MethodSNP array
Analysis1) We applied common software Birdsuite to detect genome-wide CNVs; 2) we used our algorithm WinXPCNVer which is based on probe intensity to identify Tibetan specific CNV; 3) we further genotyped the discovered Tibetan specific CNV by K-means and manual observation.
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceLou_et_al_2015
Pubmed ID26073780
Accession Number(s)nsv1159884
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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