A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1161390



Internal ID19302784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109700332..109703659hg38UCSC Ensembl
Outerchr1:109697556..109707613hg38UCSC Ensembl
Innerchr1:110242954..110246281hg19UCSC Ensembl
Outerchr1:110240178..110250235hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810058
hg1910058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv17n111
Supporting Variantsnssv4041056, nssv4041053, nssv4041052, nssv4041055, nssv4041054
Samples
Known Genes
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)nsv1161390
Frequency
Sample Size369
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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