A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160617



Internal ID19303636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39866378..39870288hg38UCSC Ensembl
Outerchr19:39860089..39873982hg38UCSC Ensembl
Innerchr19:40357018..40360928hg19UCSC Ensembl
Outerchr19:40350729..40364622hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3813894
hg1913894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4039824
Samples
Known GenesFCGBP
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)nsv1160617
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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