A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546242



Internal ID18400632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:94773965..94774238hg38UCSC Ensembl
Outerchr5:94773925..94774246hg38UCSC Ensembl
Innerchr10:47088425..47088698hg19UCSC Ensembl
Outerchr10:47088358..47088741hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38322
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744989
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546242
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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