A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160899



Internal ID19304008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:206359983..206368391hg38UCSC Ensembl
Outerchr2:206355420..206377369hg38UCSC Ensembl
Innerchr2:207224707..207233115hg19UCSC Ensembl
Outerchr2:207220144..207242093hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3821950
hg1921950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4027540
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)nsv1160899
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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