A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160113



Internal ID19303440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55108037..55131769hg38UCSC Ensembl
Outerchr13:55105061..55138436hg38UCSC Ensembl
Innerchr13:55682172..55705904hg19UCSC Ensembl
Outerchr13:55679196..55712571hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3833376
hg1933376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4031675
Samples
Known Genes
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)nsv1160113
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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