A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160755



Internal ID19304340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35515968..35524087hg38UCSC Ensembl
Outerchr22:35512420..35527058hg38UCSC Ensembl
Innerchr22:35912015..35920134hg19UCSC Ensembl
Outerchr22:35908467..35923105hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3814639
hg1914639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4040776
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)nsv1160755
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer