A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601149



Internal ID16388558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24322059..24327273hg38UCSC Ensembl
Innerchr6:24322287..24327501hg19UCSC Ensembl
Innerchr6:24430266..24435480hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg385215
hg195215
hg185215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10327n54
Supporting Variantsnssv1051247
Samples
Known GenesDCDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601149
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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