A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561357



Internal ID18415747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2591356..2591654hg38UCSC Ensembl
Outerchr3:2591290..2591722hg38UCSC Ensembl
Innerchr3:2633040..2633338hg19UCSC Ensembl
Outerchr3:2632974..2633406hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760104
Samples
Known GenesCNTN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561357
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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