A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4039716



Internal ID18955169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10627898..10888774hg38UCSC Ensembl
Outerchr19:10618877..10892186hg38UCSC Ensembl
Innerchr19:10738574..10999450hg19UCSC Ensembl
Outerchr19:10729553..11002862hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38273310
hg19273310
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1160584
Supporting Variants
Samples
Known GenesC19orf38, CARM1, DNM2, ILF3, ILF3-AS1, MIR199A1, MIR4748, MIR638, MIR6793, QTRT1, SLC44A2, TMED1
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)nssv4039716
Frequency
Sample Size369
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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