A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542059



Internal ID18743135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89890984..89899686hg38UCSC Ensembl
Outerchr7:89889687..89901686hg38UCSC Ensembl
Innerchr7:89520298..89529000hg19UCSC Ensembl
Outerchr7:89519001..89531000hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3812000
hg1912000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740806
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542059
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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