A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160436



Internal ID18957792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77172399..77188969hg38UCSC Ensembl
Outerchr16:77167588..77193772hg38UCSC Ensembl
Innerchr16:77206296..77222866hg19UCSC Ensembl
Outerchr16:77201485..77227669hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3826185
hg1926185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv125n111
Supporting Variantsnssv4038989
Samples
Known GenesMON1B
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)nsv1160436
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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