A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160156



Internal ID19303460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19667065..19955213hg38UCSC Ensembl
Outerchr14:19650668..19956767hg38UCSC Ensembl
Innerchr14:20135224..20423372hg19UCSC Ensembl
Outerchr14:20118883..20424926hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38306100
hg19306044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv87n111
Supporting Variantsnssv4031763, nssv4031764
Samples
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
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)nsv1160156
Frequency
Sample Size369
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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