A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160585



Internal ID18956747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10678137..10769271hg38UCSC Ensembl
Outerchr19:10674243..10771056hg38UCSC Ensembl
Innerchr19:10788813..10879947hg19UCSC Ensembl
Outerchr19:10784919..10881732hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3896814
hg1996814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4039717
Samples
Known GenesDNM2, ILF3, MIR638, QTRT1
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)nsv1160585
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer