A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10908n54



Internal ID20144332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110248622..110250090hg38UCSC Ensembl
chr6:110569825..110571293hg19UCSC Ensembl
chr6:110676518..110677986hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381469
hg191469
hg181469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604501, nsv604503, nsv604502, nsv604504
Samples
Known GenesMETTL24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10908n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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