A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1159770



Internal ID19304574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120091011..120106457hg38UCSC Ensembl
Outerchr10:120085744..120108699hg38UCSC Ensembl
Innerchr10:121850523..121865969hg19UCSC Ensembl
Outerchr10:121845256..121868211hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3822956
hg1922956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4030195
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)nsv1159770
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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