A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156019



Internal ID22086524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132273929..132276840hg38UCSC Ensembl
Outerchr3:132273893..132281633hg38UCSC Ensembl
Innerchr3:131992773..131995684hg19UCSC Ensembl
Outerchr3:131992737..132000477hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387741
hg197741
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015838, nssv4015881, nssv4015848, nssv4015863, nssv4015893, nssv4015879, nssv4015887, nssv4015855, nssv4015868, nssv4015841, nssv4015870, nssv4015856, nssv4015890, nssv4015845, nssv4015878, nssv4015851, nssv4015894, nssv4015860, nssv4015843, nssv4015852, nssv4015842, nssv4015875, nssv4015866, nssv4015886, nssv4015891, nssv4015859, nssv4015846, nssv4015880, nssv4015861, nssv4015885, nssv4015857, nssv4015888, nssv4015877, nssv4015892, nssv4015853, nssv4015849, nssv4015854, nssv4015883, nssv4015869, nssv4015850, nssv4015847, nssv4015889, nssv4015836, nssv4015876, nssv4015858, nssv4015882, nssv4015865, nssv4015873, nssv4015867, nssv4015871, nssv4015862, nssv4015844, nssv4015874, nssv4015840, nssv4015839, nssv4015895, nssv4015864, nssv4015884, nssv4015872, nssv4015837
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156019
Frequency
Sample Size131
Observed Gain1
Observed Loss59
Observed Complex0
Frequencyn/a


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