A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540273



Internal ID18394663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106535765..106536061hg38UCSC Ensembl
Outerchr6:106535723..106536093hg38UCSC Ensembl
Innerchr6:106983640..106983936hg19UCSC Ensembl
Outerchr6:106983598..106983968hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739020
Samples
Known GenesAIM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540273
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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