A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744911



Internal ID18719157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35878810..35885072hg38UCSC Ensembl
Outerchr10:35877906..35885187hg38UCSC Ensembl
Innerchr10:36167738..36174000hg19UCSC Ensembl
Outerchr10:36166834..36174115hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg387282
hg197282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744911
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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