A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541686



Internal ID18742762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55342168..55342409hg38UCSC Ensembl
Outerchr7:55342155..55342449hg38UCSC Ensembl
Innerchr7:55409861..55410102hg19UCSC Ensembl
Outerchr7:55409848..55410142hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9740433
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541686
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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