A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1161500



Internal ID19304575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11876379..11910435hg38UCSC Ensembl
Outerchr7:11874472..11911322hg38UCSC Ensembl
Innerchr7:11916005..11950061hg19UCSC Ensembl
Outerchr7:11914098..11950948hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3836851
hg1936851
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4035320
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)nsv1161500
Frequency
Sample Size369
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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