A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744590



Internal ID18718836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6612855..6621538hg38UCSC Ensembl
Outerchr10:6611339..6622538hg38UCSC Ensembl
Innerchr10:6654817..6663500hg19UCSC Ensembl
Outerchr10:6653301..6664500hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3811200
hg1911200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744590
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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