A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761818



Internal ID18736064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189858172..189858424hg38UCSC Ensembl
Outerchr3:189858051..189858479hg38UCSC Ensembl
Innerchr3:189575961..189576213hg19UCSC Ensembl
Outerchr3:189575840..189576268hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563071
Supporting Variants
Samples
Known GenesTP63
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761818
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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