A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051247



Internal ID15904433
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 StatusS
Merged Variantsnsv601149
Supporting Variants
Samples
Known GenesDCDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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