A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1161031



Internal ID18955915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8200971..8250128hg38UCSC Ensembl
Outerchr4:8200484..8254225hg38UCSC Ensembl
Innerchr4:8202698..8251855hg19UCSC Ensembl
Outerchr4:8202211..8255952hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3853742
hg1953742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4028520
Samples
Known GenesSH3TC1
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)nsv1161031
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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