A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3539955



Internal ID18741031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71861740..71862047hg38UCSC Ensembl
Outerchr6:71861682..71862083hg38UCSC Ensembl
Innerchr6:72571443..72571750hg19UCSC Ensembl
Outerchr6:72571385..72571786hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv394e215
Supporting Variantsessv9738702
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3539955
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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