A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1161371



Internal ID18957634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109681762..109700331hg38UCSC Ensembl
Outerchr1:109679105..109702376hg38UCSC Ensembl
Innerchr1:110224384..110242953hg19UCSC Ensembl
Outerchr1:110221727..110244998hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3823272
hg1923272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv16n111
Supporting Variantsnssv4041005, nssv4040978, nssv4029719, nssv4040985, nssv4029701, nssv4040986, nssv4029700, nssv4041006, nssv4029693, nssv4029712, nssv4029708, nssv4041023, nssv4041026, nssv4040999, nssv4041012, nssv4041017, nssv4041024, nssv4040990, nssv4040982, nssv4041042, nssv4029691, nssv4029727, nssv4041030, nssv4041040, nssv4029697, nssv4029726, nssv4029714, nssv4040987, nssv4041034, nssv4029723, nssv4029717, nssv4041036, nssv4029694, nssv4029720, nssv4029703, nssv4041002, nssv4029715, nssv4029716, nssv4041038, nssv4040997, nssv4041020, nssv4041041, nssv4041008, nssv4040991, nssv4041003, nssv4029710, nssv4041031, nssv4029724, nssv4041021, nssv4029690, nssv4041000, nssv4029722, nssv4029692, nssv4029689, nssv4041035, nssv4040992, nssv4040980, nssv4040996, nssv4041011, nssv4040984, nssv4041025, nssv4029725, nssv4041022, nssv4029706, nssv4041039, nssv4029711, nssv4040983, nssv4029699, nssv4041010, nssv4041032, nssv4040993, nssv4040994, nssv4041007, nssv4041009, nssv4040998, nssv4029695, nssv4041018, nssv4041033, nssv4040995, nssv4041001, nssv4040989, nssv4041037, nssv4041028, nssv4041004, nssv4041029, nssv4029702, nssv4029709, nssv4041014, nssv4041027, nssv4041015, nssv4029705, nssv4029713, nssv4029704, nssv4040981, nssv4040988, nssv4041019, nssv4029688, nssv4041016, nssv4040979, nssv4029698, nssv4029721, nssv4041013
Samples
Known GenesGSTM1, GSTM2
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)nsv1161371
Frequency
Sample Size369
Observed Gain0
Observed Loss102
Observed Complex0
Frequencyn/a


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