A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11067n54



Internal ID22778962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168316451..168317857hg38UCSC Ensembl
chr6:168717131..168718537hg19UCSC Ensembl
chr6:168459980..168461386hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381407
hg191407
hg181407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605467, nsv605462, nsv605464, nsv605463
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11067n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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