A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058268



Internal ID19147487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45719911..45749572hg38UCSC Ensembl
Innerchr20:44348550..44378211hg19UCSC Ensembl
Innerchr20:43781964..43811618hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3829662
hg1929662
hg1829655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n100
Supporting Variantsnssv3737220, nssv3584888, nssv3584885, nssv3731325, nssv3584882, nssv3584865, nssv3737221, nssv3584858, nssv3584862, nssv3737217, nssv3731324, nssv3731323, nssv3584887, nssv3584886, nssv3737225, nssv3584855, nssv3584850, nssv3584859, nssv3584878, nssv3737219, nssv3584869, nssv3584853, nssv3584872, nssv3737218, nssv3584863, nssv3731329, nssv3584875, nssv3584876, nssv3731331, nssv3731327, nssv3584883, nssv3731332, nssv3731330, nssv3584884, nssv3584871, nssv3584856, nssv3731333, nssv3584861, nssv3731335, nssv3584860, nssv3584857, nssv3737226, nssv3737222, nssv3584867, nssv3584868, nssv3584874, nssv3584879, nssv3584880, nssv3584877, nssv3737216, nssv3584854, nssv3584864, nssv3584873, nssv3584881, nssv3731326, nssv3584890, nssv3584889, nssv3584852, nssv3737215, nssv3584851, nssv3584866, nssv3731328, nssv3584870, nssv3731334, nssv3737223, nssv3737224, nssv3584891
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058268
Frequency
Sample Size11257
Observed Gain0
Observed Loss67
Observed Complex0
Frequencyn/a


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