A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738835



Internal ID18713023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85663432..85664201hg38UCSC Ensembl
Outerchr6:85663245..85664231hg38UCSC Ensembl
Innerchr6:86373150..86373919hg19UCSC Ensembl
Outerchr6:86372963..86373949hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738835
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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