A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4038117



Internal ID18953570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34977856..35046530hg38UCSC Ensembl
Outerchr10:34971581..35049745hg38UCSC Ensembl
Innerchr10:35266784..35335458hg19UCSC Ensembl
Outerchr10:35260509..35338673hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3878165
hg1978165
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1161937
Supporting Variants
Samples
Known GenesCUL2
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)nssv4038117
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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