A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602078



Internal ID16389487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32017441..32023513hg38UCSC Ensembl
Innerchr6:31985218..31991290hg19UCSC Ensembl
Innerchr6:32093196..32099268hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386073
hg196073
hg186073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10480n54
Supporting Variantsnssv1053841, nssv1053833, nssv1053846, nssv1053826, nssv1053849, nssv1053842, nssv1053832, nssv1053830, nssv1053828, nssv1053836, nssv1053850, nssv1053848, nssv1053838, nssv1053839, nssv1053845, nssv1053843, nssv1053840, nssv1053837, nssv1053829, nssv1053835, nssv1053831, nssv1053834, nssv1053844, nssv1053827, nssv1053847
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)nsv602078
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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