A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160735



Internal ID18956114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23940829..23990739hg38UCSC Ensembl
Outerchr22:23929558..23995113hg38UCSC Ensembl
Innerchr22:24283016..24332933hg19UCSC Ensembl
Outerchr22:24271745..24337307hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3865556
hg1965563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4040588
Samples
Known GenesDDT, DDTL, GSTT2, GSTT2B
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)nsv1160735
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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