A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1160472



Internal ID19302802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41053891..41066554hg38UCSC Ensembl
Outerchr17:41047659..41069285hg38UCSC Ensembl
Innerchr17:39210143..39222806hg19UCSC Ensembl
Outerchr17:39203911..39225537hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3821627
hg1921627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127n111
Supporting Variantsnssv4039207
Samples
Known GenesKRTAP2-2, KRTAP2-3, KRTAP2-4
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)nsv1160472
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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