A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601259



Internal ID16041982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29945738hg38UCSC Ensembl
Innerchr6:29851443..29913515hg19UCSC Ensembl
Innerchr6:29959422..30021494hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3862073
hg1962073
hg1862073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10347n54
Supporting Variantsnssv1051794, nssv1051795
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601259
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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