A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023381



Internal ID19112598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..381137hg38UCSC Ensembl
Innerchr6:302294..381137hg19UCSC Ensembl
Innerchr6:247294..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3878844
hg1978844
hg1878844
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5890n100
Supporting Variantsnssv3653767, nssv3653781, nssv3653806, nssv3653805, nssv3747846, nssv3747868, nssv3653795, nssv3747860, nssv3747855, nssv3653769, nssv3653804, nssv3747852, nssv3653787, nssv3747851, nssv3653780, nssv3653802, nssv3653784, nssv3653772, nssv3747858, nssv3747848, nssv3747853, nssv3653789, nssv3653774, nssv3653788, nssv3747862, nssv3653801, nssv3653798, nssv3653776, nssv3653800, nssv3653777, nssv3653773, nssv3653786, nssv3653771, nssv3747856, nssv3653783, nssv3653793, nssv3653779, nssv3747859, nssv3653762, nssv3747866, nssv3747847, nssv3653799, nssv3747865, nssv3653794, nssv3653785, nssv3653768, nssv3653807, nssv3653790, nssv3747861, nssv3653763, nssv3747849, nssv3653791, nssv3653782, nssv3747857, nssv3747863, nssv3747850, nssv3747867, nssv3653796, nssv3747864, nssv3653775, nssv3747869, nssv3747871, nssv3747854, nssv3653765, nssv3653803, nssv3747845, nssv3653778, nssv3653764, nssv3747870, nssv3653766, nssv3653792, nssv3653797, nssv3653770
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023381
Frequency
Sample Size11257
Observed Gain65
Observed Loss8
Observed Complex0
Frequencyn/a


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