A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594768



Internal ID16382177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86056124..86058774hg38UCSC Ensembl
Innerchr4:86977277..86979927hg19UCSC Ensembl
Innerchr4:87196301..87198951hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg382651
hg192651
hg182651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9147n54
Supporting Variantsnssv1002691, nssv1002667, nssv1002696, nssv1002682, nssv1002676, nssv1002671, nssv1002684, nssv1002713, nssv1002710, nssv1002687, nssv1002674, nssv1002661, nssv1002665, nssv1002703, nssv1002689, nssv1002694, nssv1002701, nssv1002707, nssv1002685, nssv1002688, nssv1002666, nssv1002700, nssv1002679, nssv1002675, nssv1002664, nssv1002658, nssv1002699, nssv1002708, nssv1002677, nssv1002709, nssv1002670, nssv1002659, nssv1002698, nssv1002690, nssv1002660, nssv1002695, nssv1002704, nssv1002693, nssv1002702, nssv1002663, nssv1002673, nssv1002692, nssv1002662, nssv1002705, nssv1002681, nssv1002686, nssv1002712, nssv1002711, nssv1002678, nssv1002706, nssv1002680, nssv1002683, nssv1002672, nssv1002669, nssv1002668, nssv1002697
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594768
Frequency
Sample Size17421
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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