A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738460



Internal ID18713127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:50484765..50485080hg38UCSC Ensembl
Outerchr6:50484693..50485136hg38UCSC Ensembl
Innerchr6:50452478..50452793hg19UCSC Ensembl
Outerchr6:50452406..50452849hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3539713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738460
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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