A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1161621



Internal ID18956729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141387830..141389186hg38UCSC Ensembl
Outerchr7:141387661..141390368hg38UCSC Ensembl
Innerchr7:141087630..141088986hg19UCSC Ensembl
Outerchr7:141087461..141090168hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382708
hg192708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv246n111
Supporting Variantsnssv4035817
Samples
Known GenesTMEM178B
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)nsv1161621
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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