A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604408



Internal ID16045131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104813034..104814546hg38UCSC Ensembl
Innerchr6:105260909..105262421hg19UCSC Ensembl
Innerchr6:105367602..105369114hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381513
hg191513
hg181513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10892n54
Supporting Variantsnssv1071776, nssv1071702, nssv1071772, nssv1071734, nssv1071710, nssv1071755, nssv1071738, nssv1071737, nssv1071794, nssv1071748, nssv1071717, nssv1071798, nssv1071807, nssv1071750, nssv1071765, nssv1071767, nssv1071744, nssv1071799, nssv1071711, nssv1071730, nssv1071746, nssv1071803, nssv1071775, nssv1071701, nssv1071729, nssv1071723, nssv1071781, nssv1071754, nssv1071736, nssv1071795, nssv1071790, nssv1071718, nssv1071694, nssv1071783, nssv1071788, nssv1071704, nssv1071706, nssv1071808, nssv1071743, nssv1071779, nssv1071735, nssv1071712, nssv1071782, nssv1071713, nssv1071778, nssv1071774, nssv1071784, nssv1071777, nssv1071700, nssv1071708, nssv1071715, nssv1071786, nssv1071785, nssv1071764, nssv1071792, nssv1071763, nssv1071802, nssv1071695, nssv1071762, nssv1071804, nssv1071709, nssv1071698, nssv1071757, nssv1071759, nssv1071719, nssv1071806, nssv1071731, nssv1071805, nssv1071732, nssv1071769, nssv1071725, nssv1071800, nssv1071753, nssv1071789, nssv1071699, nssv1071722, nssv1071749, nssv1071740, nssv1071770, nssv1071707, nssv1071726, nssv1071780, nssv1071766, nssv1071787, nssv1071761, nssv1071697, nssv1071728, nssv1071745, nssv1071716, nssv1071801, nssv1071758, nssv1071696, nssv1071739, nssv1071760, nssv1071752, nssv1071727, nssv1071720, nssv1071791, nssv1071724, nssv1071693, nssv1071747, nssv1071714, nssv1071751, nssv1071705, nssv1071793, nssv1071773, nssv1071703, nssv1071797, nssv1071771, nssv1071741, nssv1071796, nssv1071742, nssv1071768, nssv1071756, nssv1071721, nssv1071733
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604408
Frequency
Sample Size17421
Observed Gain0
Observed Loss116
Observed Complex0
Frequencyn/a


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