A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160762



Internal ID18956425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39219312..39294317hg38UCSC Ensembl
Outerchr22:39214849..39298220hg38UCSC Ensembl
Innerchr22:39615317..39690322hg19UCSC Ensembl
Outerchr22:39610854..39694225hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3883372
hg1983372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4040872
Samples
Known GenesPDGFB
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)nsv1160762
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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