A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738774



Internal ID18712962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77644679..77647139hg38UCSC Ensembl
Outerchr6:77644464..77647517hg38UCSC Ensembl
Innerchr6:78354396..78356856hg19UCSC Ensembl
Outerchr6:78354181..78357234hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383054
hg193054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540027
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738774
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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