A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602041



Internal ID16389450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31996100..31996613hg38UCSC Ensembl
Innerchr6:31963877..31964390hg19UCSC Ensembl
Innerchr6:32071839..32072370hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38514
hg19514
hg18532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053758, nssv1053736, nssv1053772, nssv1053747, nssv1053746, nssv1053763, nssv1053760, nssv1053743, nssv1053749, nssv1053756, nssv1053761, nssv1053755, nssv1053754, nssv1053732, nssv1053737, nssv1053771, nssv1053734, nssv1053735, nssv1053770, nssv1053739, nssv1053767, nssv1053745, nssv1053742, nssv1053753, nssv1053759, nssv1053769, nssv1053775, nssv1053776, nssv1053774, nssv1053738, nssv1053773, nssv1053751, nssv1053757, nssv1053750, nssv1053765, nssv1053764, nssv1053766, nssv1053777, nssv1053748, nssv1053752, nssv1053744, nssv1053740, nssv1053733, nssv1053762, nssv1053741, nssv1053768
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602041
Frequency
Sample Size17421
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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