A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4034907



Internal ID19298770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76766568..76773069hg38UCSC Ensembl
Outerchr6:76766568..76778010hg38UCSC Ensembl
Innerchr6:77476285..77482786hg19UCSC Ensembl
Outerchr6:77476285..77487727hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3811443
hg1911443
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1161419
Supporting Variants
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)nssv4034907
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer