A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160608



Internal ID18955900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358159..35376052hg38UCSC Ensembl
Outerchr19:35356251..35379446hg38UCSC Ensembl
Innerchr19:35849061..35866954hg19UCSC Ensembl
Outerchr19:35847153..35870348hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3823196
hg1923196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n111
Supporting Variantsnssv4039770, nssv4039769
Samples
Known GenesFFAR3
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)nsv1160608
Frequency
Sample Size369
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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