A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1161433



Internal ID19304227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93318764..93353299hg38UCSC Ensembl
Outerchr6:93313004..93358780hg38UCSC Ensembl
Innerchr6:94028482..94063017hg19UCSC Ensembl
Outerchr6:94022722..94068498hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3845777
hg1945777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4034953
Samples
Known GenesEPHA7
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)nsv1161433
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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