A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739053



Internal ID18366596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110248536..110250639hg38UCSC Ensembl
Outerchr6:110248508..110250712hg38UCSC Ensembl
Innerchr6:110569739..110571842hg19UCSC Ensembl
Outerchr6:110569711..110571915hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540306
Supporting Variants
Samples
Known GenesMETTL24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739053
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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