A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv266n111



Internal ID22798466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39368830..39537590hg38UCSC Ensembl
chr8:39226349..39395109hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38168761
hg19168761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1161752, nsv1161754, nsv1161751, nsv1161750, nsv1161755, nsv1161757, nsv1161756, nsv1161753
Samples
Known GenesADAM3A, ADAM5
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)dgv266n111
Frequency
Sample Size369
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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