A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760317



Internal ID18734563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20968556..20972007hg38UCSC Ensembl
Outerchr3:20967804..20972061hg38UCSC Ensembl
Innerchr3:21010048..21013499hg19UCSC Ensembl
Outerchr3:21009296..21013553hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384258
hg194258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760317
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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