A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540282



Internal ID18741358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107710226..107711140hg38UCSC Ensembl
Outerchr6:107709990..107711268hg38UCSC Ensembl
Innerchr6:108031430..108032344hg19UCSC Ensembl
Outerchr6:108031194..108032472hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381279
hg191279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739029
Samples
Known GenesSCML4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540282
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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