A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546094



Internal ID18400484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29453386..29454019hg38UCSC Ensembl
Outerchr10:29453241..29454079hg38UCSC Ensembl
Innerchr10:29742315..29742948hg19UCSC Ensembl
Outerchr10:29742170..29743008hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38839
hg19839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744841
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546094
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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