A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065860



Internal ID19155079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18685360..18708616hg38UCSC Ensembl
Innerchr21:20057678..20080934hg19UCSC Ensembl
Innerchr21:18979549..19002805hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3823257
hg1923257
hg1823257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599768, nssv3599780, nssv3732651, nssv3599776, nssv3599754, nssv3599762, nssv3732643, nssv3732642, nssv3732661, nssv3599759, nssv3599793, nssv3599792, nssv3599772, nssv3732655, nssv3732653, nssv3599761, nssv3732660, nssv3732644, nssv3599775, nssv3732649, nssv3599751, nssv3599752, nssv3599803, nssv3732646, nssv3732662, nssv3732664, nssv3732666, nssv3732650, nssv3599798, nssv3599777, nssv3599778, nssv3599767, nssv3599805, nssv3732659, nssv3732656, nssv3732645, nssv3732637, nssv3732668, nssv3599801, nssv3599773, nssv3599791, nssv3599755, nssv3732638, nssv3599769, nssv3599764, nssv3599758, nssv3732641, nssv3732663, nssv3599788, nssv3599753, nssv3732667, nssv3732640, nssv3599784, nssv3599779, nssv3599763, nssv3599804, nssv3599774, nssv3599787, nssv3599770, nssv3599799, nssv3599766, nssv3599781, nssv3599806, nssv3599789, nssv3599800, nssv3599802, nssv3732639, nssv3599771, nssv3732647, nssv3599760, nssv3732652, nssv3599797, nssv3599795, nssv3599807, nssv3599794, nssv3732648, nssv3599790, nssv3732658, nssv3599786, nssv3599782, nssv3599756, nssv3732665, nssv3599757, nssv3599765, nssv3599750, nssv3732669, nssv3732654, nssv3599785, nssv3732657, nssv3599796, nssv3599783
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)nsv1065860
Frequency
Sample Size11257
Observed Gain91
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer