A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11024n54



Internal ID20144448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163403832..163415602hg38UCSC Ensembl
chr6:163824864..163836634hg19UCSC Ensembl
chr6:163744854..163756624hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3811771
hg1911771
hg1811771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605193, nsv605195, nsv605194
Samples
Known GenesCAHM, QKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11024n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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