A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540069



Internal ID18741145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82800773..82801772hg38UCSC Ensembl
Outerchr6:82800751..82801997hg38UCSC Ensembl
Innerchr6:83510490..83511489hg19UCSC Ensembl
Outerchr6:83510468..83511714hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9738816
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540069
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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