A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601343



Internal ID16042066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29893694..29917019hg38UCSC Ensembl
Innerchr6:29861471..29884796hg19UCSC Ensembl
Innerchr6:29969450..29992775hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3823326
hg1923326
hg1823326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10349n54
Supporting Variantsnssv1051992, nssv1051993
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601343
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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