A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10460n54



Internal ID20143884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31489401..31507709hg38UCSC Ensembl
chr6:31457178..31475486hg19UCSC Ensembl
chr6:31565157..31583465hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3818309
hg1918309
hg1818309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601937, nsv601939, nsv601938
Samples
Known GenesMICB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10460n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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