A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567456



Internal ID18768532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27070675..27070728hg38UCSC Ensembl
chr6:27038454..27038507hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766203
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567456
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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