A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061985



Internal ID19151204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27474595hg38UCSC Ensembl
Innerchr19:27747981..27965503hg19UCSC Ensembl
Innerchr19:32439821..32657343hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38217523
hg19217523
hg18217523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3496n100
Supporting Variantsnssv3570851, nssv3570857, nssv3570833, nssv3570854, nssv3570847, nssv3570835, nssv3570836, nssv3570828, nssv3570843, nssv3570839, nssv3570850, nssv3570849, nssv3570840, nssv3570831, nssv3570837, nssv3570842, nssv3570846, nssv3570855, nssv3570845, nssv3570853, nssv3570829, nssv3570838, nssv3570832, nssv3570844, nssv3570830, nssv3570856, nssv3570834, nssv3570852, nssv3570848, nssv3570841
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061985
Frequency
Sample Size11257
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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