A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160746



Internal ID19302794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40572072..40629121hg38UCSC Ensembl
Outerchr2:40566740..40633279hg38UCSC Ensembl
Innerchr2:40799212..40856261hg19UCSC Ensembl
Outerchr2:40793880..40860419hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3866540
hg1966540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4026531
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)nsv1160746
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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