A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545893



Internal ID18746969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10767840..10768009hg38UCSC Ensembl
Outerchr10:10767833..10768010hg38UCSC Ensembl
Innerchr10:10809803..10809972hg19UCSC Ensembl
Outerchr10:10809796..10809973hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744640
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545893
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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